2-[(Thiazol-2-yl)methylthio]ethylamine → 3-[2-(2-Thiazolylmethylthio)ethylamino]-6-(3-pyridylmethyl)-1,2,4-triazin-5-one

HRID 27220

反応式

HRID 27220 の反応式
CS[C:3]1[NH:8][C:7](=[O:9])[C:6]([CH2:10][C:11]2[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=2)=[N:5][N:4]=1.[S:17]1[CH:21]=[CH:20][N:19]=[C:18]1[CH2:22][S:23][CH2:24][CH2:25][NH2:26]>>[S:17]1[CH:21]=[CH:20][N:19]=[C:18]1[CH2:22][S:23][CH2:24][CH2:25][NH:26][C:3]1[NH:8][C:7](=[O:9])[C:6]([CH2:10][C:11]2[CH:12]=[N:13][CH:14]=[CH:15][CH:16]=2)=[N:5][N:4]=1

参加物

3

反応物 2

HCID 129234032-[(Thiazol-2-yl)methylthio]ethylamineHCID 1357554243-Methylthio-6-(3-pyridylmethyl)-1,2,4-triazin-5-one

生成物 1

HCID 1357031853-[2-(2-Thiazolylmethylthio)ethylamino]-6-(3-pyridylmethyl)-1,2,4-triazin-5-one

実験手順

3-Methylthio-6-(3-pyridylmethyl)-1,2,4-triazin-5-one (3.28 g) and 2-(2-thiazolylmethylthio)ethylamine (2.7 g) were heated together on an oil bath (160°-170°) for 1 hour. The cooled mixture was triturated with isopropanol and the solid was twice recrystallised from ethanol to give the title compound as pale yellow plates (3.1 g) m.p. 158°-59°.

後処理

  1. customThe cooled mixture was triturated with isopropanol
  2. customthe solid was twice recrystallised from ethanol

出典と根拠

ORDレコード
ord-555d7dc55d5f40cab2687d3c206b6437
出典データセット
uspto-grants-1980_09
特許番号
US04220767

関連ノート

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