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

Ammonia → HCID 21293088, 화합물

HRID 622385
노트
인쇄 미리보기

반응식

HRID 622385 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][CH2:9][CH2:10][CH2:11][NH2:12])=[N:6][CH:7]=1.CO[C:15]1[C:19](OC)=[N:18][S:17](=[O:22])[N:16]=1.[NH3:23]>CO>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][CH2:9][CH2:10][CH2:11][NH:12][C:15]2[C:19]([NH2:23])=[N:18][S:17](=[O:22])[N:16]=2)=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 222AmmoniaHCID 107281442-N-(3-Aminopropyl)-amino-5-bromopyridineHCID 129139473,4-Dimethoxy-1,2,5-thiadiazole 1-oxide

생성물 1

HCID 21293088HCID 21293088, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

A solution of 3-(5-bromopyrid-2-ylamino)propylamine (1 g) and 3,4-dimethoxy-1,2,5-thiadiazole-1-oxide (0.71 g) was stirred in methanol for 3 hours. Methanol saturated with ammonia (10 ml) was added and the solution was stirred for 18 hours, concentrated in vacuo and the residue was chromatographed on silica eluted with 10% v:v methanol in chloroform followed by recrystallisation from methanol to give 3-[3-(5-bromopyrid-2-ylamino)propylamino]-4-amino-1,2,5-thiadiazole-1-oxide (0.63 g), m.p. 215°-216° C.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. concentrationconcentrated in vacuo
  2. customthe residue was chromatographed on silica
  3. washeluted with 10% v
  4. customv methanol in chloroform followed by recrystallisation from methanol

출처 및 근거

ORD 기록
ord-07ca96ad95334a79bd7a644b7595fcb8
출처 데이터셋
uspto-grants-1988_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04771058

반응 노트

불러오는 중…