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

Acetic Anhydride → HCID 18180200, 화합물

HRID 1383311
노트
인쇄 미리보기

반응식

HRID 1383311 반응식
[NH2:1][C:2]1[C:7]([Br:8])=[N:6][CH:5]=[C:4]([NH2:9])[N:3]=1.[C:10](OC(=O)C)(=[O:12])[CH3:11]>COC(OC)C>[NH2:1][C:2]1[C:7]([Br:8])=[N:6][CH:5]=[C:4]([NH:9][C:10](=[O:12])[CH3:11])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 18180211HCID 18180211, 화합물

생성물 1

HCID 18180200HCID 18180200, 화합물

시약·촉매·용매 1

HCID 107951,1-Dimethoxyethane용매

실험 절차

A mixture of 2,6-diamino-3-bromopyrazine (10.50 g, 0.056 mole) in dry 1,1-dimethoxyethane (168 ml) and acetic anhydride (7.91 ml, 8.56 g, 0.084 mole) was refluxed under nitrogen for 2.50 hrs. The cooled mixture was evaporated in vacuo. The residue was triturated with ether, filtered and dried in vacuo. Yield 10.31 g (80%), M.p. 218-221° C.

후처리

  1. temperaturewas refluxed under nitrogen for 2.50 hrs
  2. customThe cooled mixture was evaporated in vacuo
  3. customThe residue was triturated with ether
  4. filtrationfiltered
  5. customdried in vacuo

출처 및 근거

ORD 기록
ord-9baf6d417fd94505879aef8f014d0fa1
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06255307B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트