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Methylamine → 1-(6-Chloro-3-pyridylmethyl)-1,3-dimethyl-2-nitroguanidine

HRID 1781593
노트
인쇄 미리보기

반응식

HRID 1781593 반응식
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][N:9]([CH3:17])[C:10](=[N:13][N+:14]([O-:16])=[O:15])SC)=[CH:4][CH:3]=1.[CH3:18][NH2:19]>C(#N)C>[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8][N:9]([CH3:17])[C:10]([NH:19][CH3:18])=[N:13][N+:14]([O-:16])=[O:15])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329MethylamineHCID 867449291-(6-Chloro-3-pyridylmethyl)-1,2-dimethyl-3-nitroisothiourea

생성물 1

HCID 1363411811-(6-Chloro-3-pyridylmethyl)-1,3-dimethyl-2-nitroguanidine수율 72.8%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
70 °C

실험 절차

A mixture of 0.82 g of 1-(6-chloro-3-pyridyl-methyl)-1,2-dimethyl-3-nitroisothiourea, 0.464 g of 40% methylamine aqueous solution and 10 ml of acetonitrile was stirred for 2 hours at 70° C., and concentrated. The residue was purified by a column chromatography developing solution: dichloromethane-methanol [10:1]) to afford 0.56 g of 1-(6-chloro-3-pyridylmethyl)-1,3-dimethyl-2-nitroguanidine (Compound No. 8).

후처리

  1. concentrationconcentrated
  2. customThe residue was purified by a column chromatography

출처 및 근거

ORD 기록
ord-cfb1593aec87497ca8ab97928a86ad43
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05633375

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