반응식
[NH2:1][CH2:2][C@@H:3]1[C@H:7]2[O:8][C:9]([CH3:12])([CH3:11])[O:10][C@H:6]2[C@H:5]([N:13]2[C:17]3[N:18]=[CH:19][N:20]=[C:21]([NH:22][CH2:23][C:24]4[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[CH:26][C:25]=4[O:32][CH3:33])[C:16]=3[CH:15]=[CH:14]2)[CH2:4]1.ClCCCl.[CH3:38][C:39]([CH3:41])=O.C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl>[CH3:33][O:32][C:25]1[CH:26]=[C:27]([O:30][CH3:31])[CH:28]=[CH:29][C:24]=1[CH2:23][NH:22][C:21]1[C:16]2[CH:15]=[CH:14][N:13]([C@H:5]3[C@H:6]4[C@H:7]([O:8][C:9]([CH3:12])([CH3:11])[O:10]4)[C@@H:3]([CH2:2][NH:1][CH:39]([CH3:41])[CH3:38])[CH2:4]3)[C:17]=2[N:18]=[CH:19][N:20]=1참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
A solution of 7((3aS,4R,6R,6aR)-6-(aminomethyl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl)-N-(2,4-dimethoxybenzyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine (7.50 g, 16.5 mmol) in 1,2-Dichloroethane (140 mL, 1800 mmol) was treated with Acetone (1.34 mL, 18.2 mmol;) and Acetic acid (0.94 mL, 16 mmol) dropwise followed by Sodium triacetoxyborohydride (4.20 g, 19.8 mmol) and the mixture was stirred at RT for 4 h. HPLC analysis indicated the reaction was complete. The reaction mixture was diluted with 200 mL CH2Cl2 and washed with 150 mL sat NaHCO3. The aqueous phase was washed with 100 mL CH2Cl2 and the combined organic phase was dried over Na2SO4, filtered and concentrated to yield a an oil that produced a stiff foam when placed under high vac. The crude material (9.3 g) was carried on directly to the next step.
후처리
- washwashed with 150 mL
- washThe aqueous phase was washed with 100 mL CH2Cl2
- dry with materialthe combined organic phase was dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customto yield a an oil that
- customproduced a stiff foam when
출처 및 근거
- ORD 기록
- ord-b6028203555f4898acd92a48e895fac6
- 출처 데이터셋
- uspto-grants-2013_11
- 특허 번호
- US08580762B2
연결된 노트
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