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

Phosphorus oxychloride → 4-Chloro-5-methyl-5,7-dihydrothieno[3,4-D]pyrimidine

HRID 625031
노트
인쇄 미리보기

반응식

HRID 625031 반응식
[CH3:1][CH:2]1[C:10]2[C:9](O)=[N:8][CH:7]=[N:6][C:5]=2[CH2:4][S:3]1.O=P(Cl)(Cl)[Cl:14]>>[Cl:14][C:9]1[C:10]2[CH:2]([CH3:1])[S:3][CH2:4][C:5]=2[N:6]=[CH:7][N:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178435045HCID 178435045, 화합물

생성물 1

HCID 717438984-Chloro-5-methyl-5,7-dihydrothieno[3,4-D]pyrimidine수율 54%

실험 절차

5-Methyl-5,7-dihydrothieno[3,4-d]pyrimidin-4-ol (10 g, 59.54 mmol) in POCl3 (100 mL) was heated to reflux for 15 minutes. After cooling, excess POCl3 was removed under vacuum. The residue was dissolved in CH2Cl2 (100 mL) and saturated NaHCO3 (400 mL) was added at 0° C. The reaction mixture was stirred for 1 hour. The aqueous phase was extracted with DCM (3×250 mL). The organic phase was combined, dried and concentrated. The residue was purified by silica gel chromatography, eluting with Hexane/ethyl acetate (4:1) to give 4-chloro-5-methyl-5,7-dihydrothieno[3,4-d]pyrimidine (6 g, 54%). 1H NMR (CDCl3, 400 MHz) δ 8.80 (s, 1H), 4.68 (m, 1H), 4.44 (m, 1H), 4.13 (d, J=16.8 Hz, 2H), 1.68 (d, J=7.2 Hz, 3H).

후처리

  1. temperatureto reflux for 15 minutes
  2. temperature
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
After cooling
  • customexcess POCl3 was removed under vacuum
  • dissolutionThe residue was dissolved in CH2Cl2 (100 mL)
  • additionsaturated NaHCO3 (400 mL) was added at 0° C
  • extractionThe aqueous phase was extracted with DCM (3×250 mL)
  • customdried
  • concentrationconcentrated
  • customThe residue was purified by silica gel chromatography
  • washeluting with Hexane/ethyl acetate (4:1)
  • 출처 및 근거

    ORD 기록
    ord-c6bffdf48d9247f8968804a9de2f8867
    출처 데이터셋
    uspto-grants-2016_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09303040B2

    반응 노트

    불러오는 중…