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Ethanol → 4-(2-Chloro-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)morpholine

HRID 928577
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인쇄 미리보기

반응식

HRID 928577 반응식
[Cl:1][C:2]1[N:3]=[C:4](Cl)[C:5]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[CH:9][S:8][C:6]=2[N:7]=1.[NH:18]1[CH2:23][CH2:22][O:21][CH2:20][CH2:19]1.C(N(CC)CC)C.C(O)C>>[Cl:1][C:2]1[N:3]=[C:4]([N:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)[C:5]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[CH:9][S:8][C:6]=2[N:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 702EthanolHCID 8083MorpholineHCID 8471TriethylamineHCID 127242282,4-Dichloro-5-phenylthieno(2,3-d)pyrimidine

생성물 1

HCID 820658184-(2-Chloro-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)morpholine

반응 조건

온도
50 °C

실험 절차

2,4-Dichloro-5-phenyl-thieno[2,3-d]pyrimidine (2 g, 7.112 mmol), morpholine (0.9294 g, 10.67 mmol) and triethylamine (1.454 g, 2.00 mL, 14.22 mmol) were combined in ethanol (23.7 g, 30 mL, 493 mmol) and heated to 50° C. for 1 hour. The reaction mixture was allowed to cool to room temperature. The solvent volume was reduced by half and the resulting precipitate filtered off and washed with water and dried in vacuo overnight at 40° C. to afford 4-(2-chloro-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)morpholine as a white solid.

후처리

  1. temperatureto cool to room temperature
  2. filtrationthe resulting precipitate filtered off
  3. washwashed with water
  4. customdried in vacuo overnight at 40° C.

출처 및 근거

ORD 기록
ord-39e52fc9d0bc49cbb12f0b778a7e8544
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09290511B2

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