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Benzyl Alcohol → N-(tert-Butoxycarbonyl)-(2S,4R)-4-fluoroproline benzyl ester

HRID 1527376
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HRID 1527376 반응식
[C:1]([N:8]1[CH2:15][C@H:14]([F:16])[CH2:13][C@H:9]1[C:10]([OH:12])=[O:11])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].C1CCC(N=C=NC2CCCCC2)CC1.[CH2:32](O)[C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1>C(Cl)Cl.CN(C1C=CN=CC=1)C>[C:4]([O:3][C:1]([N:8]1[CH2:15][C@H:14]([F:16])[CH2:13][C@H:9]1[C:10]([O:12][CH2:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:11])=[O:2])([CH3:7])([CH3:6])[CH3:5]
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참가 물질

6

반응물 3

HCID 244Benzyl AlcoholHCID 10868DicyclohexylcarbodiimideHCID 12043048(2S,4R)-1-[(tert-butoxy)carbonyl]-4-fluoropyrrolidine-2-carboxylic acid

생성물 1

HCID 68554319N-(tert-Butoxycarbonyl)-(2S,4R)-4-fluoroproline benzyl ester

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매
HCID 6344
Dichloromethane
용매

실험 절차

To a suspension of N-Boc-trans-4-fluoro-L-proline (4.5 g, 19.29 mmol) in CH2Cl2 (68 mL) were added DCC (4.78 g, 23.15 mmol), DMAP (0.236 g, 1.93 mmol) and benzyl alcohol (2 mL, 19.29 mmol). The resulting white suspension was stirred at RT for 48 h and filtered. The filtrate was concentrated to give a colorless oil which was purified by flash column chromatography on silica gel (c-hexane to c-hexane/EtOAc 4-1) to give the desired compound. TLC, Rf (c-hexane/EtOAc 3:1)=0.3; MS: 346.0 [M+Na]+; tR (HPLC conditions a): 3.85 min.

후처리

  1. filtrationfiltered
  2. concentrationThe filtrate was concentrated
  3. customto give a colorless oil which
  4. customwas purified by flash column chromatography on silica gel (c-hexane to c-hexane/EtOAc 4-1)

출처 및 근거

ORD 기록
ord-890d4d9ea2e646c681ccb6cd502039f6
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085555B2

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