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

Butyl chloroformate → 2-Amino-1-n-butoxycarbonyl-4,5-dicyanoimidazole

HRID 1576950
노트
인쇄 미리보기

반응식

HRID 1576950 반응식
[NH2:1][C:2]1[NH:3][C:4]([C:9]#[N:10])=[C:5]([C:7]#[N:8])[N:6]=1.C(=O)(O)[O-].[Na+].Cl[C:17]([O:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:18]>CC(C)=O>[NH2:1][C:2]1[N:3]([C:17]([O:19][CH2:20][CH2:21][CH2:22][CH3:23])=[O:18])[C:4]([C:9]#[N:10])=[C:5]([C:7]#[N:8])[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 61140Butyl chloroformateHCID 1704461H-Imidazole-4,5-dicarbonitrile, 2-amino-HCID 516892Sodium Bicarbonate

생성물 1

HCID 102202732-Amino-1-n-butoxycarbonyl-4,5-dicyanoimidazole

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

2 g of 2-amino-4,5-dicyanoimidazole was dissolved in 20 ml of suspension of acetone containing 1.3 g of sodium bicarbonate and then 2.1 g of n-butyl chloroformate was added dropwise to said solution at a room temperature. The resulting solution was refluxed during 30 minutes, and white crystal was separated out when the rection mixture was poured into ice-water. After recrystallizing the crude product from methanol, 2.7 g of the purified compound having a melting point of 170° to 172°C was obtained as needles (Yield rate: 77%).

후처리

  1. customat a room temperature
  2. temperatureThe resulting solution was refluxed during 30 minutes
  3. customwhite crystal was separated out when the rection mixture
  4. additionwas poured into ice-water
  5. customAfter recrystallizing the crude product from methanol, 2.7 g of the purified compound
  6. customwas obtained as needles (Yield rate: 77%)

출처 및 근거

ORD 기록
ord-74a95b4112994c06a0bccf0a4f944f1f
출처 데이터셋
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03983241

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트