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Potassium tert-butoxide → HCID 68838475, 화합물

HRID 660765
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HRID 660765 반응식
[NH2:1][S:2]([N:5]([C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][C:19](=[O:27])[O:20][CH2:21][CH2:22][Si:23]([CH3:26])([CH3:25])[CH3:24])=[CH:13][C:12]=1[O:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[CH2:6][C:7](OC)=[O:8])(=[O:4])=[O:3].CC(C)([O-])C.[K+]>C1COCC1>[CH3:24][Si:23]([CH3:26])([CH3:25])[CH2:22][CH2:21][O:20][C:19](=[O:27])[CH2:18][O:17][C:14]1[CH:15]=[CH:16][C:11]([N:5]2[CH2:6][C:7](=[O:8])[NH:1][S:2]2(=[O:4])=[O:3])=[C:12]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 23665647Potassium tert-butoxideHCID 68840538Methyl N-(aminosulfonyl)-N-(2-(benzyloxy)-4-{2-oxo-2-[2-(trimethylsilyl)ethoxy]ethoxy}phenyl)glycinate

생성물 1

HCID 68838475HCID 68838475, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of methyl N-(aminosulfonyl)-N-(2-(benzyloxy)-4-{2-oxo-2-[2-(trimethylsilyl)ethoxy]ethoxy}phenyl)glycinate in THF is added potassium t-butoxide (1.1 equivalent) in THF dropwise. The mixture is stirred at RT for 18 h. The solvent is removed under reduced pressure to afford the title compound which is used directly in the next step.

후처리

  1. customThe solvent is removed under reduced pressure

출처 및 근거

ORD 기록
ord-0e59aa6acd894632ac7d2a82f4f6c89a
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08084448B2

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