Triethylamine → HCID 59475009, 화합물
반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@:8]2([OH:16])[CH2:13][CH2:12][NH:11][CH2:10][C:9]2([CH3:15])[CH3:14])=[CH:4][CH:3]=1.[C:17]([O:21][C:22]([NH:24][C@H:25]1[CH2:28][CH2:27][C@H:26]1[C:29](O)=[O:30])=[O:23])([CH3:20])([CH3:19])[CH3:18].C(N(CC)CC)C.F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@:8]2([OH:16])[CH2:13][CH2:12][N:11]([C:29]([C@H:26]3[CH2:27][CH2:28][C@H:25]3[NH:24][C:22](=[O:23])[O:21][C:17]([CH3:19])([CH3:18])[CH3:20])=[O:30])[CH2:10][C:9]2([CH3:14])[CH3:15])=[CH:4][CH:3]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of (S)-4-(4-chlorophenyl)-3,3-dimethylpiperidin-4-ol (91 mg, 0.381 mmol), (±)-(cis)-2-(tert-butoxycarbonylamino)cyclobutanecarboxylic acid (82 mg, 0.381 mmol), and triethylamine (0.186 mL, 1.333 mmol) in methylene chloride (5 mL) was treated with BOP (168 mg, 0.381 mmol), and the mixture was stirred overnight at room temperature. At the conclusion of this period, the solvent was evaporated with a stream of nitrogen, and the resulting residue was taken up in ethyl acetate. The resulting mixture was washed 3× with saturated sodium carbonate, 3× with 1 N HCl, once with water, and once with brine, then the organic phase was concentrated in vacuo to yield the title compound (160 mg, 96% yield) as a colorless glass. The material was used as-is without further purification. MS (ESI+)=437.4 (M+H)+.
후처리
- customAt the conclusion of this period, the solvent was evaporated with a stream of nitrogen
- washThe resulting mixture was washed 3× with saturated sodium carbonate, 3× with 1 N HCl
- concentrationonce with water, and once with brine, then the organic phase was concentrated in vacuo
출처 및 근거
- ORD 기록
- ord-08f1dd65681040e4a09cb0d057b36abd
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08536198B2
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