2-Chloro-3-ethyl-4-fluorobenzonitrile → 2-Chloro-3-ethyl-4-[[(1S)-2-hydroxy-2-methyl-cyclopentyl]amino]benzonitrile
반응식
Cl.[NH2:2][C@H:3]1[CH2:7][CH2:6][CH2:5][C:4]1([CH3:9])[OH:8].[Cl:10][C:11]1[C:18]([CH2:19][CH3:20])=[C:17](F)[CH:16]=[CH:15][C:12]=1[C:13]#[N:14]>>[Cl:10][C:11]1[C:18]([CH2:19][CH3:20])=[C:17]([NH:2][C@H:3]2[CH2:7][CH2:6][CH2:5][C:4]2([OH:8])[CH3:9])[CH:16]=[CH:15][C:12]=1[C:13]#[N:14]참가 물질
3
실험 절차
2-Chloro-3-ethyl-4-[[(1S)-2-hydroxy-2-methyl-cyclopentyl]amino]benzonitrile is prepared essentially as described in Example 1 using (2S)-2-amino-1-methyl-cyclopentanol hydrochloride (Preparation 18) and 2-chloro-3-ethyl-4-fluoro-benzonitrile. The crude material (350 mg) is purified using silica gel chromatography (20-60% EtOAc/hexane) to obtain Diastereomer 1 (cis) (82 mg) and Diastereomer 2 (trans) (29 mg).
후처리
- customThe crude material (350 mg) is purified
- customto obtain Diastereomer 1 (cis) (82 mg) and Diastereomer 2 (trans) (29 mg)
출처 및 근거
- ORD 기록
- ord-b91f345106b04b868e0f65ce672534ab
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08658693B2
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