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Dimethylformamide → HCID 86649018, 화합물

HRID 1367466
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HRID 1367466 반응식
[CH2:1]([O:3][C:4]([C@@H:6]1[CH2:10][C:9](=[O:11])[CH2:8][C@H:7]1[C:12](=[O:17])[NH:13][CH2:14][C:15]#[N:16])=[O:5])[CH3:2].CN(C=O)C.[BH4-].[Na+]>C1COCC1>[CH2:1]([O:3][C:4]([C@@H:6]1[CH2:10][C@H:9]([OH:11])[CH2:8][C@H:7]1[C:12](=[O:17])[NH:13][CH2:14][C:15]#[N:16])=[O:5])[CH3:2]
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 4311764Sodium borohydrideHCID 86649017HCID 86649017, 화합물

생성물 1

HCID 86649018HCID 86649018, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

To a suspension of (1R,2R)-2-(cyanomethyl-carbamoyl)-4-oxo-cyclopentanecarboxylic acid ethyl ester (2.7 mmol) in THF (12 ml) was added DMF (1 ml), the solution was cooled to 0° C., sodium borohydride (3.3 mmol) was added and stirring was continued for 2 h. The mixture was partitioned between 1N aqueous HCl and ethyl acetate, the organic layer was dried, evaporated and the residue chromatographed on silica using dichloromethane/MeOH (97:3) to give in the first fraction (1R,2R,4R)-2-(cyanomethyl-carbamoyl)-4-hydroxy-cyclopentanecarboxylic acid ethyl ester as a white solid. MS: 241.4 (M+H)+. The second fraction contained the desired isomer,

후처리

  1. customThe mixture was partitioned between 1N aqueous HCl and ethyl acetate
  2. customthe organic layer was dried
  3. customevaporated
  4. customthe residue chromatographed on silica

출처 및 근거

ORD 기록
ord-88058659d051422faeebefb41ccbaee5
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07893099B2

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