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

Isopropanol → 5-(3-Fluoro-pyridin-4-yl)-1H-pyrimidine-2,4-dione hydrochloride

HRID 12696
노트
인쇄 미리보기

반응식

HRID 12696 반응식
[F:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[C:8]1[C:9]([O:16]C)=[N:10][C:11]([O:14]C)=[N:12][CH:13]=1.CC(O)C.C(Cl)[Cl:23]>CO>[ClH:23].[F:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[C:8]1[C:9](=[O:16])[NH:10][C:11](=[O:14])[NH:12][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 6344DichloromethaneHCID 589941815-(3-Fluoro-pyridin-4-yl)-2,4-dimethoxy-pyrimidine

생성물 1

HCID 686942765-(3-Fluoro-pyridin-4-yl)-1H-pyrimidine-2,4-dione hydrochloride수율 85%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 5-(3-Fluoro-pyridin-4-yl)-2,4-dimethoxy-pyrimidine (Prep 66, 725 mg, 3.1 mmol) in MeOH (50 ml) 2N HClaq (20 ml) was added. After refluxing the mixture for 1 hour, the solvents were evaporated and the crude was tritured with hexane then with iPrOH and finally with DCM to give 550 mg of the title compound (85% yield)

후처리

  1. temperatureAfter refluxing the mixture for 1 hour
  2. customthe solvents were evaporated

출처 및 근거

ORD 기록
ord-f57bbcdae829410bbe9f1eaea270f0fb
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07727988B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트