Benzyl Chloride → 2-Amino-5-dibenzylaminomethylpyrrolo[2,3-d]pyrimidin-4-one

HRID 1903314노트

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HRID 1903314 반응식
[NH2:1][C:2]1[N:7]=[C:6]2[N:8]=[CH:9][C:10]([CH2:11][NH:12][CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[C:5]2[C:4](=[O:20])[N:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:27](Cl)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>CO.[I-].[Na+]>[NH2:1][C:2]1[N:7]=[C:6]2[N:8]=[CH:9][C:10]([CH2:11][N:12]([CH2:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)=[C:5]2[C:4](=[O:20])[N:3]=1

참가 물질

6

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온도
60 °C

실험 절차

In 30 ml of methanol was dissolved 172 mg of 2-amino-5-benzylaminomethylpyrrolo[2,3-d]pyrimidin-4-one (the compound of Example 4), followed by addition of 90 mg of anhydrous potassium carbonate, 2 mg of sodium iodide and 81 mg of benzyl chloride. The mixture was stirred on a water bath at 60° C. for 4 hrs. The solvent was then distilled off and the residue was purified by silica gel column chromatography to give 57 mg of the desired compound.

후처리

  1. distillationThe solvent was then distilled off
  2. customthe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-502030615bf548bc96bcac359d882794
출처 데이터셋
uspto-grants-1984_03
특허 번호
US04435569

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