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拉莫三嗪

CAS 84057-84-1C9H7Cl2N5MW 256.09

拉莫三嗪(CAS 84057-84-1):分子式 C9H7Cl2N5、分子量 256.09。

产品概览

CAS号84057-84-1
分子式C9H7Cl2N5
分子量256.09
熔点177-181
沸点503.1±60.0
LogP1.93
应用领域Uses: MEDICATION、Anticonvulsants、Calcium Channel Blockers、Excitatory Amino Acid Antagonists、Voltage-Gated Sodium Channel Blockers、Use (kg) in Switzerland (2009): >1000、Use (kg、approx.) in Germany (2009): >7500、Use (kg) in USA (2002): 10500、Consumption (g per capita) in Switzerland (2009): 0.13、Consumption (g per capita、approx.) in Germany (2009): 0.092、Consumption (g per capita) in the USA (2002): 0.037、Excretion rate: 0.1、Calculated removal (%): 11、For the adjunctive treatment of partial seizures in epilepsy and generalized seizures of Lennox-Gastaut syndrome. Also for the maintenance treatment of bipolar I disorder and depression. Off-label uses include the treatment of peripheral neuropathy、trigeminal neuralgia、cluster headaches、migraines、and reducing neuropathic pain. (A308、L1155)、Use Classification: Pharmaceuticals、Methods of Manufacturing: Reaction of 2、3-dichlorobenzoyl chloride with cyanide ion forms the benzoylcyanide derivative that is then treated with aminoguanidine to form a Schiff base through loss of water between the carbonyl group and the one primary amine function of the guanidine. Ring closure by addition of the lone free primary amino group remaining on the guanidine moiety of the nitrile function is accomplished by base catalysis and yields the product.、The reaction of the Grignard compound of 2、3-dichloroiodobenzene with CO2 in diethyl ether gives 2、3-dichlorobenzoic acid、which is converted to the corresponding acyl chloride by refluxing with SOCl2. The reaction of 2、3-dichlorobenzoyl chloride with cuprous cyanide and KI in refluxing xylene yields 2、3-dichlorobenzoyl cyanide. Finally、this compound is cyclized with aminoguanidine in DMSO to yield lamotrigine.、Hydrogenation of 2、3-dichloronitrobenzene with H2 over Raney nickel in methanol gives 2、3-dichloroaniline、which is diazotized with NaNO2 and HCl and treated with CuCN to yield 2、3-dichlorobenzonitrile. Hydrolysis of the nitrile with NaOH in refluxing methanol、water affords 2、which is treated with hot SOCl2 to provide the corresponding acyl chloride. Reaction of 2、3-dichlorobenzoyl chloride with CuCN and KI in refluxing chlorobenzene gives 2、3-dichlorobenzoyl cyanide、which is condensed with aminoguanidine by means of H2SO4、TsOH in hot toluene to yield 2、3-dichlorobenzoyl cyanide amidinohydrazone. Finally、this compound is cyclized by treatment with NaOMe in refluxing methanol to yield lamotrigine.、Preparation: M. G. Baxter et al.、European Patent Office patent 21121 (1981 to Wellcome Foundation)、D. A. Sawyer et al.、USA patent 4602017 (1986).、Formulations、Preparations: Table: Lamotrigine Preparations [Table#7220]

应用领域

登记用途:Uses: MEDICATION、Anticonvulsants、Calcium Channel Blockers、Excitatory Amino Acid Antagonists、Voltage-Gated Sodium Channel Blockers、Use (kg) in Switzerland (2009): >1000、Use (kg、approx.) in Germany (2009): >7500、Use (kg) in USA (2002): 10500、Consumption (g per capita) in Switzerland (2009): 0.13、Consumption (g per capita、approx.) in Germany (2009): 0.092、Consumption (g per capita) in the USA (2002): 0.037、Excretion rate: 0.1、Calculated removal (%): 11、For the adjunctive treatment of partial seizures in epilepsy and generalized seizures of Lennox-Gastaut syndrome. Also for the maintenance treatment of bipolar I disorder and depression. Off-label uses include the treatment of peripheral neuropathy、trigeminal neuralgia、cluster headaches、migraines、and reducing neuropathic pain. (A308、L1155)、Use Classification: Pharmaceuticals、Methods of Manufacturing: Reaction of 2、3-dichlorobenzoyl chloride with cyanide ion forms the benzoylcyanide derivative that is then treated with aminoguanidine to form a Schiff base through loss of water between the carbonyl group and the one primary amine function of the guanidine. Ring closure by addition of the lone free primary amino group remaining on the guanidine moiety of the nitrile function is accomplished by base catalysis and yields the product.、The reaction of the Grignard compound of 2、3-dichloroiodobenzene with CO2 in diethyl ether gives 2、3-dichlorobenzoic acid、which is converted to the corresponding acyl chloride by refluxing with SOCl2. The reaction of 2、3-dichlorobenzoyl chloride with cuprous cyanide and KI in refluxing xylene yields 2、3-dichlorobenzoyl cyanide. Finally、this compound is cyclized with aminoguanidine in DMSO to yield lamotrigine.、Hydrogenation of 2、3-dichloronitrobenzene with H2 over Raney nickel in methanol gives 2、3-dichloroaniline、which is diazotized with NaNO2 and HCl and treated with CuCN to yield 2、3-dichlorobenzonitrile. Hydrolysis of the nitrile with NaOH in refluxing methanol、water affords 2、which is treated with hot SOCl2 to provide the corresponding acyl chloride. Reaction of 2、3-dichlorobenzoyl chloride with CuCN and KI in refluxing chlorobenzene gives 2、3-dichlorobenzoyl cyanide、which is condensed with aminoguanidine by means of H2SO4、TsOH in hot toluene to yield 2、3-dichlorobenzoyl cyanide amidinohydrazone. Finally、this compound is cyclized by treatment with NaOMe in refluxing methanol to yield lamotrigine.、Preparation: M. G. Baxter et al.、European Patent Office patent 21121 (1981 to Wellcome Foundation)、D. A. Sawyer et al.、USA patent 4602017 (1986).、Formulations、Preparations: Table: Lamotrigine Preparations [Table#7220]。

技术档案

这个产品是什么

拉莫三嗪 是一种化工化合物,登记 CAS 号为 84057-84-1,分子式 C9H7Cl2N5(分子量 256.09)。

识别信息

登记 CAS 号:84057-84-1

其分子式 C9H7Cl2N5 由 9 个碳、7 个氢、2 个氯、5 个氮 组成。

别名/同义词:拉莫三嗪 · Lamotrigine

常见问题

拉莫三嗪 的 CAS 号是多少?

拉莫三嗪 的 CAS 登记号为 84057-84-1。

拉莫三嗪 的分子式与分子量是多少?

分子式 C9H7Cl2N5,分子量 256.09。

拉莫三嗪 还有哪些别名?

别名/同义词:拉莫三嗪、Lamotrigine。

拉莫三嗪 的登记用途是什么?

登记用途:Uses: MEDICATION、Anticonvulsants、Calcium Channel Blockers、Excitatory Amino Acid Antagonists、Voltage-Gated Sodium Channel Blockers、Use (kg) in Switzerland (2009): >1000、Use (kg、approx.) in Germany (2009): >7500、Use (kg) in USA (2002): 10500、Consumption (g per capita) in Switzerland (2009): 0.13、Consumption (g per capita、approx.) in Germany (2009): 0.092、Consumption (g per capita) in the USA (2002): 0.037、Excretion rate: 0.1、Calculated removal (%): 11、For the adjunctive treatment of partial seizures in epilepsy and generalized seizures of Lennox-Gastaut syndrome. Also for the maintenance treatment of bipolar I disorder and depression. Off-label uses include the treatment of peripheral neuropathy、trigeminal neuralgia、cluster headaches、migraines、and reducing neuropathic pain. (A308、L1155)、Use Classification: Pharmaceuticals、Methods of Manufacturing: Reaction of 2、3-dichlorobenzoyl chloride with cyanide ion forms the benzoylcyanide derivative that is then treated with aminoguanidine to form a Schiff base through loss of water between the carbonyl group and the one primary amine function of the guanidine. Ring closure by addition of the lone free primary amino group remaining on the guanidine moiety of the nitrile function is accomplished by base catalysis and yields the product.、The reaction of the Grignard compound of 2、3-dichloroiodobenzene with CO2 in diethyl ether gives 2、3-dichlorobenzoic acid、which is converted to the corresponding acyl chloride by refluxing with SOCl2. The reaction of 2、3-dichlorobenzoyl chloride with cuprous cyanide and KI in refluxing xylene yields 2、3-dichlorobenzoyl cyanide. Finally、this compound is cyclized with aminoguanidine in DMSO to yield lamotrigine.、Hydrogenation of 2、3-dichloronitrobenzene with H2 over Raney nickel in methanol gives 2、3-dichloroaniline、which is diazotized with NaNO2 and HCl and treated with CuCN to yield 2、3-dichlorobenzonitrile. Hydrolysis of the nitrile with NaOH in refluxing methanol、water affords 2、which is treated with hot SOCl2 to provide the corresponding acyl chloride. Reaction of 2、3-dichlorobenzoyl chloride with CuCN and KI in refluxing chlorobenzene gives 2、3-dichlorobenzoyl cyanide、which is condensed with aminoguanidine by means of H2SO4、TsOH in hot toluene to yield 2、3-dichlorobenzoyl cyanide amidinohydrazone. Finally、this compound is cyclized by treatment with NaOMe in refluxing methanol to yield lamotrigine.、Preparation: M. G. Baxter et al.、European Patent Office patent 21121 (1981 to Wellcome Foundation)、D. A. Sawyer et al.、USA patent 4602017 (1986).、Formulations、Preparations: Table: Lamotrigine Preparations [Table#7220]。

PubChem 公开数据

拉莫三嗪(CAS 84057-84-1)的独立参考数据,整理自公开化学数据库。

各数据库的登记标识

CAS 号84057-84-1
PubChem CID3878
分子式C9H7Cl2N5
IUPAC 名称6-(2,3-dichlorophenyl)-1,2,4-triazine-3,5-diamine
UNII(FDA)U3H27498KS

计算分子描述符

Molecular Weight256.09
XLogP31.4
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count1
Exact Mass255.0078506
Monoisotopic Mass255.0078506
Topological Polar Surface Area90.7
Heavy Atom Count16

在册的理化数值

Boiling Point503.1±60.0
Melting Point177-181
Melting Point216-218 °C (uncorr)
Melting Point216 - 218 °C (uncorr.)
Solubility0.17
SolubilityIn water, 170 mg/L at 25 °C
Solubility4.88e-01 g/L
LogP1.93
LogPlog Kow = 2.57
LogP2.5

同义词与商品名

lamotrigine; 84057-84-1; 6-(2,3-Dichlorophenyl)-1,2,4-triazine-3,5-diamine; Lamictal; Lamictal Cd; Lamotrigina; Lamictal XR; Lamotriginum; BW 430C; 3,5-Diamino-6-(2,3-dichlorophenyl)-1,2,4-triazine; BW-430C; Lamictal ODT; 1,2,4-Triazine-3,5-diamine, 6-(2,3-dichlorophenyl)-; 3,5-Diamino-6-(2,3-dichlorophenyl)-as-triazine; DTXSID2023195; BW430C

GHS 危害分类

已通报的危害声明H301 (100%), H412 (19.1%), H319 (100%), H336 (100%), H361 (100%), H362 (100%), H410 (100%)

公开数据库对它的描述

拉莫三嗪 · CAS 84057-84-1 · C9H7Cl2N5. UNII U3H27498KS. Boiling Point: 503.1±60.0; Melting Point: 177-181; Melting Point: 216-218 °C (uncorr).

数据来源:PubChem / Wikidata;与随货 COA 不一致时以 COA 为准。

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