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Borane → HCID 69428429, 화합물

HRID 1006847
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HRID 1006847 반응식
[CH3:1][O:2][C:3]([CH:5]1[CH2:10][CH2:9][CH:8]([C:11](O)=[O:12])[CH2:7][N:6]1[S:14]([CH3:17])(=[O:16])=[O:15])=[O:4].B>O1CCCC1>[CH3:1][O:2][C:3]([CH:5]1[CH2:10][CH2:9][CH:8]([CH2:11][OH:12])[CH2:7][N:6]1[S:14]([CH3:17])(=[O:15])=[O:16])=[O:4]
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참가 물질

4

반응물 2

HCID 6331BoraneHCID 69433575(2RS,5RS)-1-methanesulfonyl-piperidine-2,5-dicarboxylic acid 2-methyl ester

생성물 1

HCID 69428429HCID 69428429, 화합물수율 79.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

To a solution of (2RS,5RS)-1-methanesulfonyl-piperidine-2,5-dicarboxylic acid 2-methyl ester (10.7 g) in tetrahydrofuran was added a 1 M borane solution in tetrahydrofuran (215 ml) within 0.5 h at 0° C. The reaction mixture was stirred for 4 h at 0° C., poured onto ice/saturated sodium bicarbonate solution and concentrated. The aqueous residue was extracted with EtOAc. The organic phase was washed with brine, dried over magnesium sulphate and concentrated. The residue was chromatographed on silica gel using EtOAc/hexane 1:1 and 3:2 as eluents to obtain (2RS,5RS)-5-hydroxymethyl-1-methanesulfonyl-piperidine-2-carboxylic acid methyl ester (8.1 g) as a colourless solid, MS: 206 (100%, M+-59).

후처리

  1. additionpoured onto ice/saturated sodium bicarbonate solution
  2. concentrationconcentrated
  3. extractionThe aqueous residue was extracted with EtOAc
  4. washThe organic phase was washed with brine
  5. dry with materialdried over magnesium sulphate
  6. concentrationconcentrated
  7. customThe residue was chromatographed on silica gel

출처 및 근거

ORD 기록
ord-0259a9700c334973af2db17808ab2a9f
출처 데이터셋
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06790860B2

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