反応式
Cl.[CH3:2][N:3](C)[OH:4].[CH2:6](N(CC)CC)C.[C:13]([O:17][C:18]([NH:20][C@@H:21]([CH2:25][CH:26]1[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1)[C:22]([OH:24])=O)=[O:19])([CH3:16])([CH3:15])[CH3:14].C(OC(Cl)=O)C(C)C.CN1CCOCC1.CN(C)O>C(Cl)Cl.C1COCC1>[CH:26]1([CH2:25][C@H:21]([NH:20][C:18](=[O:19])[O:17][C:13]([CH3:14])([CH3:15])[CH3:16])[C:22]([N:3]([O:4][CH3:6])[CH3:2])=[O:24])[CH2:31][CH2:30][CH2:29][CH2:28][CH2:27]1参加物
反応物 6
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of dimethylhydroxylamine hydrochloride (3.98 g, 40.6 mmol) in DCM (50 mL) at 0° C. was added triethylamine (5.43 mL, 41.9 mmol). In a separate flask (S)-2-((tert-butoxycarbonyl)amino)-3-cyclohexylpropanoic acid (10.0 g, 36.9 mmol) in DCM (50 mL) and THF (50 mL) was cooled to 0° C. and isobutylchloroformate (4.83 mL, 36.9 mmol) was added followed by N-methylmorpholine (4.06 mL, 36.9 mmol). After 1 h it was added to the dimethylhydroxylamine mixture. The combined mixture was allowed to warm to ambient temperature over 16 h at which time it was quenched with water, washed with sodium bicarbonate (sat.), extracted with EtOAc (2×), washed with brine, dried with sodium sulfate, filtered, and concentrated. (S)-tert-Butyl (3-cyclohexyl-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate (12.2 g) was provided as a colorless oil that was carried forward without further purification. MS (EI) for C16H30N2O4, found 215.3 [M-Boc]+.
後処理
- customwas quenched with water
- washwashed with sodium bicarbonate (sat.)
- extractionextracted with EtOAc (2×)
- washwashed with brine
- dry with materialdried with sodium sulfate
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-e82ad99134884c27bdbe5bbb99139203
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434761B2
関連ノート
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