Tributylstannane → BENZYL 4-OXO-2-[[(PHENYLMETHOXY)CARBONYL]AMINO]BUTANOATE
반응식
[NH:1]([C:17]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=[O:18])[C@H:2]([C:7]([O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:8])[CH2:3][C:4](=O)[OH:5].C(Cl)(=O)C(Cl)=O.C([SnH](CCCC)CCCC)CCC>CN(C=O)C>[CH2:10]([O:9][C:7](=[O:8])[CH:2]([NH:1][C:17]([O:19][CH2:20][C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)=[O:18])[CH2:3][CH:4]=[O:5])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1참가 물질
실험 절차
To a solution of Z-Asp-OBn (10 g, 0.028 mol) in MC (200 ml), oxalyl chloride (2.93 ml, 0.0336 mol) and a catalytic amount of DMF were added at 0° C. and stirred at room temperature for 2 hrs. After the solvent was evaporated, the crude acyl chloride was dissolved in benzene (400 ml), and tributyltin hydride (15.1 ml, 0.056 mol) and a catalytic amount of Pd(0) were added slowly at 0° C. and stirred at room temperature overnight. After the solvent was evaporated, ether (100 ml)/10% KF in water (100 ml) was added and stirred at room temperature for 2 hrs, followed by filtration to give a biphasic solution. The organic layer was separated and concentrated to give a crude product, which was purified by column chromatography to obtain the title compound, Z-Asp-OBn aldehyde (6 g) as pale-yellow oil.
후처리
- customAfter the solvent was evaporated
- dissolutionthe crude acyl chloride was dissolved in benzene (400 ml)
- stirringstirred at room temperature overnight
- customAfter the solvent was evaporated
- additionether (100 ml)/10% KF in water (100 ml) was added
- stirringstirred at room temperature for 2 hrs
- filtrationfollowed by filtration
- customto give a biphasic solution
- customThe organic layer was separated
- concentrationconcentrated
- customto give a crude product, which
- customwas purified by column chromatography
출처 및 근거
- ORD 기록
- ord-94edc024db3f49ccad71ef43ff1c1247
- 출처 데이터셋
- uspto-grants-2010_02
- 특허 번호
- US07662960B2
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