반응식
N[C:2]1[CH:3]=[C:4]([CH:21]=[CH:22][CH:23]=1)[CH2:5][N:6]1[C:10]2=[N:11][C:12]([NH2:20])=[N:13][C:14]([C:15]3[O:16][CH:17]=[CH:18][CH:19]=3)=[C:9]2[CH:8]=[N:7]1.[S:24]1[CH:28]=[CH:27][CH:26]=[C:25]1[S:29](Cl)(=[O:31])=[O:30].O.[N:34]1C=CC=CC=1>>[NH2:20][C:12]1[N:11]=[C:10]2[N:6]([CH2:5][C:4]3[CH:3]=[C:2]([C:26]4[CH:27]=[CH:28][S:24][C:25]=4[S:29]([NH2:34])(=[O:31])=[O:30])[CH:23]=[CH:22][CH:21]=3)[N:7]=[CH:8][C:9]2=[C:14]([C:15]2[O:16][CH:17]=[CH:18][CH:19]=2)[N:13]=1참가 물질
5
실험 절차
A solution of 1-(3-aminobenzyl)-4-(2-furyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine (153 mg, 0.5 mmol) in pyridine (2 mL) was treated with 2-thiophenesulphonyl chloride (91 mg, 0.5 mmol), stirred at room temperature for 16 h, poured into water, extracted with EtOAc, dried (MgSO4), concentrated in vacuo and purified by chromatography (MeOH:DCM, 1:99) to give the title compound (49 mg, 22%) as a cream solid.
후처리
- extractionextracted with EtOAc
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- custompurified by chromatography (MeOH:DCM, 1:99)
출처 및 근거
- ORD 기록
- ord-df00543d4c174ad98bde971596d1cfc6
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07087754B2
연결된 노트
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