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

Hydrochloric Acid → N-((2-aminothiazol-4-yl)methyl)-N,3-dimethylpyrazine-2-carboxamide

HRID 1685027
노트
인쇄 미리보기

반응식

HRID 1685027 반응식
[CH3:1][N:2]([CH2:12][C:13]1[N:14]=[C:15]([NH:18]C(=O)OC(C)(C)C)[S:16][CH:17]=1)[C:3]([C:5]1[C:6]([CH3:11])=[N:7][CH:8]=[CH:9][N:10]=1)=[O:4].Cl>O1CCOCC1>[NH2:18][C:15]1[S:16][CH:17]=[C:13]([CH2:12][N:2]([CH3:1])[C:3]([C:5]2[C:6]([CH3:11])=[N:7][CH:8]=[CH:9][N:10]=2)=[O:4])[N:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86661290tert-butyl 4-((N,2-dimethylpyrazine-3-carboxamido)methyl)thiazol-2-ylcarbamate

생성물 1

HCID 86661291N-((2-aminothiazol-4-yl)methyl)-N,3-dimethylpyrazine-2-carboxamide수율 116%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

실험 절차

A solution of tert-butyl 4-((N,2-dimethylpyrazine-3-carboxamido)methyl)thiazol-2-ylcarbamate (1.30 g, 3.6 mmol) in dioxane (10 mL) was treated with 4N HCl in dioxane (10 mL) for 2 hours. The resulting suspension was concentrated in vacuo to afford N-((2-aminothiazol-4-yl)methyl)-N,3-dimethylpyrazine-2-carboxamide (1.10 g).

후처리

  1. concentrationThe resulting suspension was concentrated in vacuo

출처 및 근거

ORD 기록
ord-efeaeaa8f8724cb0adcfc45b28ebe939
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08148380B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트