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

Dimethylformamide → HCID 86667820, 화합물

HRID 1772060
노트
인쇄 미리보기

반응식

HRID 1772060 반응식
[CH3:1][C:2]1[N:7]2[N:8]=[C:9]([CH:11]([CH3:16])[CH2:12][C:13](O)=[O:14])[N:10]=[C:6]2[C:5]([CH3:17])=[N:4][CH:3]=1.C(Cl)(=O)C([Cl:21])=O.CN(C=O)C>C(Cl)Cl>[CH3:1][C:2]1[N:7]2[N:8]=[C:9]([CH:11]([CH3:16])[CH2:12][C:13]([Cl:21])=[O:14])[N:10]=[C:6]2[C:5]([CH3:17])=[N:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 68089388HCID 68089388, 화합물

생성물 1

HCID 86667820HCID 86667820, 화합물수율 96%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 3-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)butanoic acid (200 mg, 0.086 mmol) in DCM (15 mL) was added oxalyl chloride (3 mL) and DMF (0.1 mL). The mixture was stirred at room temperature for 2 h. The mixture was then evaporated under reduced pressure to give the product as a brown solid (208 mg, 96% yield).

후처리

  1. customThe mixture was then evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-f5378ab99342422bacf28317783f96c5
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09249162B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트