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

N-methyl-2-pyrrolidone → 6-chloropyrazine-2-carboxamide

HRID 1670668
노트
인쇄 미리보기

반응식

HRID 1670668 반응식
[Cl:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=O)[CH:5]=[N:4][CH:3]=1.C[N:12]1C(=O)CCC1.ClC(OCC(C)C)=O.[NH4+].[OH-]>CN(C=O)C>[Cl:1][C:2]1[N:7]=[C:6]([C:8]([NH2:12])=[O:10])[CH:5]=[N:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 13387N-methyl-2-pyrrolidoneHCID 14923Ammonium HydroxideHCID 62365Isobutyl chloroformateHCID 145008756-Chloropyrazine-2-carboxylic acid

생성물 1

HCID 12825296-chloropyrazine-2-carboxamide수율 34%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
-20 °C

실험 절차

A solution of 6-chloro-pyrazine carboxylic acid (2.00 g, 12.62 mmol) in DMF (7 mL) was cooled to −40° C. NMP (2.77 mL, 25.23 mmol) and isobutyl chloroformate 3.27 mL, 25.23 mmol) were added. The temperature was allowed to increase to −20° C. during 20 min and then NH4OH was added. A precipitate was rapidly formed and after 15 min it was filtered off and washed with water. Crystallization from EtOH gave the title compound (670 mg, 34%) as light-brown needles.

후처리

  1. customA precipitate was rapidly formed and after 15 min it
  2. filtrationwas filtered off
  3. washwashed with water
  4. customCrystallization from EtOH

출처 및 근거

ORD 기록
ord-33ab6d8102cd4e9ea026058c8acacab9
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994179B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트