Potassium Iodide → 4'-{3-[(3R)-3-hydroxypyrrolidinyl]propoxy}[1,1'-biphenyl]-4-carbonitrile
반응식
N[C@@H:2]1[CH2:6][CH2:5][N:4]([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[CH:19][CH:18]=3)=[CH:13][CH:12]=2)[CH2:3]1.N1CC[C@@H]([OH:30])C1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CC(=O)CC>[OH:30][C@@H:2]1[CH2:6][CH2:5][N:4]([CH2:7][CH2:8][CH2:9][O:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[CH:19][CH:18]=3)=[CH:13][CH:12]=2)[CH2:3]1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
4′-{3-[(3R)-3-Aminopyrrolidinyl]propoxy}[1,1′-biphenyl]-4-carbonitrile (200 mg, 0.74 mmol), (3R)-3-pyrrolidinol (70 mg, 0.81 mmol), potassium carbonate (152 mg) and potassium iodide (183 mg) in 25 mL of 2-butanone were heated at 110° C. for 72 hours. The mixture was evaporated under reduced pressure and the residue was purified by chromatography (CHCl3:MeOH:NH4OH, 9:1:0.1) to provide the title compound (69 % yield).
후처리
- customThe mixture was evaporated under reduced pressure
- customthe residue was purified by chromatography (CHCl3:MeOH:NH4OH, 9:1:0.1)
출처 및 근거
- ORD 기록
- ord-3013b6033efd4cd2b031c7c502e51a06
- 출처 데이터셋
- uspto-grants-2003_02
- 특허 번호
- US06515013B2
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