Water → Tert-butyl 1-((4-(4-(3-aminopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oate
반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[N:20]([CH2:23][CH2:24][CH2:25][O:26][C:27]1[CH:62]=[CH:61][C:30]([C:31]([C:33]2[CH:38]=[CH:37][C:36]([NH:39][CH2:40][CH2:41][O:42][CH2:43][CH2:44][O:45][CH2:46][CH2:47][O:48][CH2:49][CH2:50][O:51][CH2:52][CH2:53][C:54]([O:56][C:57]([CH3:60])([CH3:59])[CH3:58])=[O:55])=[CH:35][CH:34]=2)=[O:32])=[CH:29][CH:28]=1)=[N+]=[N-].O>CCOCC.C1COCC1>[NH2:20][CH2:23][CH2:24][CH2:25][O:26][C:27]1[CH:62]=[CH:61][C:30]([C:31]([C:33]2[CH:38]=[CH:37][C:36]([NH:39][CH2:40][CH2:41][O:42][CH2:43][CH2:44][O:45][CH2:46][CH2:47][O:48][CH2:49][CH2:50][O:51][CH2:52][CH2:53][C:54]([O:56][C:57]([CH3:58])([CH3:60])[CH3:59])=[O:55])=[CH:35][CH:34]=2)=[O:32])=[CH:29][CH:28]=1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
Triphenylphosphine (2.62 g, 10.0 mmol) was added to a solution of tert-butyl 1-((4-(4-(3-azidopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oate (5.0 g 8.32 mmol) in Ether:THF (1:1, 50 mL) at 0° C. followed by of water (500 mg, 27.8 mmol). The reaction was stirred at r.t. overnight. Upon completion, the reaction was concentrated and purified by silica gel chromatography (EtOAc to EtOAc:MeOH gradient with 1% TEA) to provide 3.24 g (5.63 mmo 68.7% yield) of tert-butyl 1-((4-(4-(3-aminopropoxy)benzoyl)phenyl)amino)-3,6,9,12-tetraoxapentadecan-15-oate as yellow oil.
후처리
- concentrationUpon completion, the reaction was concentrated
- custompurified by silica gel chromatography (EtOAc to EtOAc:MeOH gradient with 1% TEA)
출처 및 근거
- ORD 기록
- ord-fcd6df3c61454f6c9a99d6c266836174
- 출처 데이터셋
- uspto-grants-2015_01
- 특허 번호
- US08933261B2
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