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

1,1'-Carbonyldiimidazole → HCID 178521918, 화합물

HRID 1588787
노트
인쇄 미리보기

반응식

HRID 1588787 반응식
[F:1][CH:2]([F:11])[C:3]1[C:7]([C:8](O)=[O:9])=[CH:6][NH:5][N:4]=1.C(N1C=CN=C1)(N1C=CN=C1)=O.[CH:24]1([C:30]2[CH:36]=[CH:35][CH:34]=[CH:33][C:31]=2[NH2:32])[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]1>C1COCC1>[CH:24]1([C:30]2[CH:36]=[CH:35][CH:34]=[CH:33][C:31]=2[NH:32][C:8]([C:7]2[C:3]([CH:2]([F:11])[F:1])=[N:4][NH:5][CH:6]=2)=[O:9])[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 682631,1'-CarbonyldiimidazoleHCID 4078992-CyclohexylbenzenamineHCID 178524804HCID 178524804, 화합물

생성물 1

HCID 178521918HCID 178521918, 화합물수율 93.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

3-(difluoromethyl)-1H-pyrazole-4-carboxylic acid (2.0 g) and 1,1'-carbonyldiimidazole (2.0 g) were mixed in THF (20mL, anhydrous) and stirred for 1 h. 2-Cyclohexylaniline (2.2 g) was added, and the contents were heated at reflux for 2 h. After cooling to RT, the contents were concentrated in vacuo leaving a foam (3.7 g). The foam was chromatographed on silica gel (Waters Prep 500) eluting with EtOAc and hexanes to give the desired amide as a white foam (750 mg). The foam was crystallized from EtOAc /pentane to give the product as a white solid (510 mg).

후처리

  1. temperaturethe contents were heated
  2. temperatureat reflux for 2 h
  3. concentrationthe contents were concentrated in vacuo

출처 및 근거

ORD 기록
ord-11da2eefc2e24dc3a0c4cd109b9c27d3
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05223526

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트