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

Dimethylformamide → HCID 178510366, 화합물

HRID 1370098
노트
인쇄 미리보기

반응식

HRID 1370098 반응식
P(Cl)(Cl)(Cl)=O.CN(C)C=O.[OH:11][C:12]1[C:20]([N+:21]([O-:23])=[O:22])=[CH:19][C:15]([C:16]([NH2:18])=O)=[CH:14][N:13]=1>O>[C:16]([C:15]1[CH:19]=[C:20]([N+:21]([O-:23])=[O:22])[C:12]([OH:11])=[N:13][CH:14]=1)#[N:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 178513756HCID 178513756, 화합물

생성물 1

HCID 178510366HCID 178510366, 화합물수율 71.8%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Phosphorus oxychloride (2.99 mL) was added dropwise to N,N-dimethylformamide (49 mL) at 0° C., and the mixture was stirred at the same temperature for 15 minutes. Then 6-hydroxy-5-nitronicotinamide (4.9 g) was added portionwise to the mixture, and the reaction mixture was stirred at 50° C. for an hour. Water was added to the reaction mixture at 0° C., and the resulting precipitate was collected by filtration in vacuo. The obtained solid was washed with water to give 5-cyano-2-hydroxy-3-nitropyridine (3.17 g) as a pale brown solid.

후처리

  1. stirringthe reaction mixture was stirred at 50° C. for an hour
  2. filtrationthe resulting precipitate was collected by filtration in vacuo
  3. washThe obtained solid was washed with water

출처 및 근거

ORD 기록
ord-31c59caaa8a0418b879aa3975ec6842f
출처 데이터셋
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06582351B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트