홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

1,1-Bis(methylthio)-2-nitroethylene → 2-(Nitromethylidene)-1-[(pyridin-4-yl)methyl]hexahydropyrimidine

HRID 1905647
노트
인쇄 미리보기

반응식

HRID 1905647 반응식
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][NH:8][CH2:9][CH2:10][CH2:11][NH2:12])=[CH:3][CH:2]=1.[N+:13]([CH:16]=[C:17](SC)SC)([O-:15])=[O:14]>CO>[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][N:8]2[CH2:9][CH2:10][CH2:11][NH:12][C:17]2=[CH:16][N+:13]([O-:15])=[O:14])=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 836231,1-Bis(methylthio)-2-nitroethyleneHCID 13576978N~1~-[(Pyridin-4-yl)methyl]propane-1,3-diamine

생성물 1

HCID 702494742-(Nitromethylidene)-1-[(pyridin-4-yl)methyl]hexahydropyrimidine수율 68.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of N-(4-pyridylmethyl)trimethylenediamine (16.5 g), 1-nitro-2,2-bis(methylthio)ethylene (16.5 g) and methanol (100 ml) was refluxed for 2 hours with stirring. The generated gas was collected by an alkali trap. The reaction mixture was cooled to room temperature, and the resulting crystals were filtered to give 1-(4-pyridylmethyl)-2-(nitromethylene)tetrahydropyrimidine (16 g) of the following formulas as pale yellow crystals. Concentrating the filtrate further gave 3 g of this compound. mp. 226°-228° C. ##STR14##

후처리

  1. temperaturewas refluxed for 2 hours
  2. customThe generated gas was collected by an alkali trap
  3. filtrationthe resulting crystals were filtered

출처 및 근거

ORD 기록
ord-cccfff14a22c462180c6e84496719ad6
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04647570

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트