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

HCID 178470495, 화합물 → HCID 178524954, 화합물

HRID 132048
노트
인쇄 미리보기

반응식

HRID 132048 반응식
C([O:3][C:4]([C:6]1[C:10]([NH:11][C:12](=[O:21])[C:13]2[C:18]([F:19])=[CH:17][CH:16]=[CH:15][C:14]=2[F:20])=[CH:9][NH:8][N:7]=1)=[O:5])C>[OH-].[Na+].CO>[F:19][C:18]1[CH:17]=[CH:16][CH:15]=[C:14]([F:20])[C:13]=1[C:12]([NH:11][C:10]1[C:6]([C:4]([OH:5])=[O:3])=[N:7][NH:8][CH:9]=1)=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 178470495HCID 178470495, 화합물

생성물 1

HCID 178524954HCID 178524954, 화합물수율 61.7%

시약·촉매·용매 1

HCID 23721981Sodium hydroxide methanol용매

실험 절차

A mixture of 4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carboxylic acid ethyl ester (10.2 g) in 2 M aqueous NaOH/MeOH (1:1, 250 ml) was stirred at ambient temperature for 14 h. Volatile materials were removed in vacuo, water (300 ml) added and the mixture taken to pH 5 using 1M aqueous HCl. The resultant precipitate was collected by filtration and dried through azeotrope with toluene to afford 4-(2,6-difluoro-benzoylamino)-1H-pyrazole-3-carboxylic acid as a pink solid (5.70 g). (LC/MS: Rt 2.33, [M+H]+267.96).

후처리

  1. customVolatile materials were removed in vacuo, water (300 ml)
addition
added
  • filtrationThe resultant precipitate was collected by filtration
  • dry with materialdried through azeotrope with toluene
  • 출처 및 근거

    ORD 기록
    ord-2be4b140c6ff4dc68478b5080f7d6a92
    출처 데이터셋
    uspto-grants-2008_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07385059B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트