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

Urea → 7-Bromo-6-fluoroquinazoline-2,4(1H,3H)-dione

HRID 2092546
노트
인쇄 미리보기

반응식

HRID 2092546 반응식
[NH2:1][C:2]1[CH:10]=[C:9]([Br:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4](O)=[O:5].[NH2:13][C:14](N)=[O:15]>O>[Br:11][C:9]1[CH:10]=[C:2]2[C:3]([C:4](=[O:5])[NH:13][C:14](=[O:15])[NH:1]2)=[CH:7][C:8]=1[F:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1176UreaHCID 675149612-Amino-4-bromo-5-fluorobenzoic acid

생성물 1

HCID 675174657-Bromo-6-fluoroquinazoline-2,4(1H,3H)-dione수율 85.8%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
200 °C

실험 절차

To a 100 mL round bottom flask, 2-amino-4-bromo-5-fluoro-benzoic acid (0.7 g, 0.003 mol) and urea (1.07 g, 0.0018 mol) were added. The reaction mixture was stirred at 200° C. for 2 h. The reaction mixture was allowed to reach 100° C. and water was added. The aqueous reaction mixture was refluxed for 5-10 min, cooled to room temperature, to get the precipitate. The solid was filtered and dried to afford the title compound (400 mg, 51%). This material was taken for next step without any further purification.

후처리

  1. customto reach 100° C.
  2. temperatureThe aqueous reaction mixture was refluxed for 5-10 min
  3. temperaturecooled to room temperature
  4. customto get the precipitate
  5. filtrationThe solid was filtered
  6. customdried

출처 및 근거

ORD 기록
ord-f8da57656e0f442f99f8dedd42b1f529
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08440662B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트