Sodium borohydride → [3-(3-Piperidin-1-yl-propoxy)-isoxazol-5-yl]-methanol

HRID 30485노트

반응식

HRID 30485 반응식
C[O:2][C:3]([C:5]1[O:9][N:8]=[C:7]([O:10][CH2:11][CH2:12][CH2:13][N:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[CH:6]=1)=O.[BH4-].[Na+]>CCO>[N:14]1([CH2:13][CH2:12][CH2:11][O:10][C:7]2[CH:6]=[C:5]([CH2:3][OH:2])[O:9][N:8]=2)[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 445154593-(3-Piperidin-1-yl-propoxy)-isoxazole-5-carboxylic acid methyl ester

생성물 1

HCID 44515460[3-(3-Piperidin-1-yl-propoxy)-isoxazol-5-yl]-methanol수율 99%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 3-(3-piperidin-1-yl-propoxy)-isoxazole-5-carboxylic acid methyl ester (0.200 g, 0.750 mmol) in EtOH (15 mL) was added NaBH4 (0.358 g, 11.2 mmol) was slowly over 30 min. The reaction mixture was heated at reflux overnight, then was cooled to rt and quenched by the addition of 1 N NaOH (10 mL). The mixture was stirred for 1 h, and then was extracted with DCM (3×30 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated to yield the desired alcohol (0.177 g, 99%). MS (ESI): exact mass calcd. for C12H20N2O3, 240.15; m/z found, 241.3 [M+H]+.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux overnight
  3. customquenched by the addition of 1 N NaOH (10 mL)
  4. extractionwas extracted with DCM (3×30 mL)
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4fb12e859a844246a266bae6761ac7a9
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07423147B2

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