Lithium Hydroxide → Benzyl 2-aminoethyl(methyl)carbamate
반응식
[CH2:1]([O:8][C:9](=[O:21])[N:10]([CH3:20])[CH2:11][CH2:12][NH:13]C(=O)C(F)(F)F)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Li+].[OH-]>CO.O>[CH2:1]([O:8][C:9](=[O:21])[N:10]([CH2:11][CH2:12][NH2:13])[CH3:20])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
실험 절차
To a solution of compound B (˜311 mmol) in MeOH (1.2 L) was added a solution of LiOH (14.9 g, 622 mmol) in water (120 mL). The reaction mixture was stirred at ambient temperature for 3 h. Solvents were evaporated to 75% of the initial volume followed by dilution with water (400 mL). The solution was extracted with EtOAc (2×300 mL). The organic layer was washed with brine (200 mL), dried over MgSO4 and evaporated in vacuo. The residue was dissolved in ether (300 mL) and treated with 2 N HCl/ether (200 mL). Formed precipitate was filtrated, washed with ether and dried in vacuo to provide the hydrochloric salt of compound C (67.8 g, 89%) as a white solid. LC-MS [M+H] 209.0 (C11H16N2O2+H, calc: 209.3). Compound C was used directly in the next reaction without purification as a DMF solution.
후처리
- customSolvents were evaporated to 75% of the initial volume
- extractionThe solution was extracted with EtOAc (2×300 mL)
- washThe organic layer was washed with brine (200 mL)
- dry with materialdried over MgSO4
- customevaporated in vacuo
- dissolutionThe residue was dissolved in ether (300 mL)
- additiontreated with 2 N HCl/ether (200 mL)
- customFormed precipitate
- filtrationwas filtrated
- washwashed with ether
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-14d0134f18b64cbd8d3fe82254101145
- 출처 데이터셋
- uspto-grants-2015_05
- 특허 번호
- US09040032B2
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