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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1,1-Bis(methylthio)-2-nitroethylene → 1-[(4-Chlorophenyl)methyl]-2-(nitromethylidene)hexahydropyrimidine

HRID 280681
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반응식

HRID 280681 반응식
[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([CH2:6][NH:7][CH2:8][CH2:9][CH2:10][NH2:11])=[CH:4][CH:3]=1.[N+:14]([CH:17]=[C:18](SC)SC)([O-:16])=[O:15]>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][N:7]2[CH2:8][CH2:9][CH2:10][NH:11][C:18]2=[CH:17][N+:14]([O-:16])=[O:15])=[CH:12][CH:13]=1
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참가 물질

4

반응물 2

HCID 836231,1-Bis(methylthio)-2-nitroethyleneHCID 2755454N-(4-Chlorobenzyl)propane-1,3-diamine

생성물 1

HCID 678444081-[(4-Chlorophenyl)methyl]-2-(nitromethylidene)hexahydropyrimidine수율 91.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

N-(4-chlorobenzyl)trimethylenediamine (8.45 g) and 1-nitro-2,2-bis(methylthio)ethylene (6.60 g) were heated under reflux in 100 ml of ethanol for 16 hours. The reaction mixture was cooled to room temperature, and the precipitated crystals were collected by filtration and washed with a small amount of ethanol to give 1-(4-chlorobenzyl)-2-(nitromethylene)tetrahydropyrimidine (9.8 g) represented by the following formula. Melting point: 172°-174° C. ##STR10##

후처리

  1. filtrationthe precipitated crystals were collected by filtration
  2. washwashed with a small amount of ethanol

출처 및 근거

ORD 기록
ord-84325f58edfd46bab40280c5617ff95f
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04590272

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