HCID 59201564、化合物 → HCID 59201605、化合物
反応式
[CH3:1][N:2]([CH2:13][C@@H:14]([NH:23]C(=O)OC(C)(C)C)[CH2:15][CH:16]1[CH2:21][CH2:20][C:19](=[O:22])[CH2:18][CH2:17]1)[C:3]([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:4]>C(O)(C(F)(F)F)=O.C(Cl)Cl>[NH2:23][C@@H:14]([CH2:15][CH:16]1[CH2:21][CH2:20][C:19](=[O:22])[CH2:18][CH2:17]1)[CH2:13][N:2]([CH3:1])[C:3](=[O:4])[O:5][CH2:6][C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1参加物
3
実験手順
(S)-tert-butyl 1-(N-methyl-N-(benzyloxycarbonyl)amino)-3-(4-oxocyclohexyl)propan-2-ylcarbamate (300 mg, 0.72 mmol) was dissolved in 5 mL of 20% TFA/CH2Cl2 and stirred 1 hr at rt. The solvent was removed to give the crude (S)-benzyl 2-amino-3-(4-oxocyclohexyl)propyl(methyl)carbamate, which was used directly for the next step without further purification.
後処理
- customThe solvent was removed
出典と根拠
- ORDレコード