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Sodium borohydride → 4-[3-(2-Hydroxymethylbenzoyl)aminopropylthio]pyridine

HRID 964129
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HRID 964129 반응식
[C:1]1(=[O:21])[N:5]([CH2:6][CH2:7][CH2:8][S:9][C:10]2[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=2)[C:4](=[O:16])[C:3]2=[CH:17][CH:18]=[CH:19][CH:20]=[C:2]12.[BH4-].[Na+]>C(O)C>[OH:21][CH2:1][C:2]1[CH:20]=[CH:19][CH:18]=[CH:17][C:3]=1[C:4]([NH:5][CH2:6][CH2:7][CH2:8][S:9][C:10]1[CH:11]=[CH:12][N:13]=[CH:14][CH:15]=1)=[O:16]
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 190791181H-Isoindole-1,3(2H)-dione, 2-[3-(4-pyridinylthio)propyl]-

생성물 1

HCID 190791424-[3-(2-Hydroxymethylbenzoyl)aminopropylthio]pyridine수율 78.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 5.97 g (20.0 mmol) of 4-(3-phthalimidopropylthio)pyridine in 300 ml of ethanol, 7.57 g (200 mmol) of sodium borohydride was added, and stirred at room temperature for 24 hours. The solvent was distilled off and saturated saline was added to the residue. The mixture was extracted with chloroform and the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10) to give 4.73 g of the desired compound (78.2% yield, colorless crystals), mp. 110°-111° C.

후처리

  1. distillationThe solvent was distilled off
  2. additionsaturated saline was added to the residue
  3. extractionThe mixture was extracted with chloroform
  4. dry with materialthe extract was dried over anhydrous magnesium sulfate
  5. distillationThe solvent was distilled off
  6. customthe residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10)

출처 및 근거

ORD 기록
ord-88ae9a98e5eb47da85f2725a55af3721
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05767121

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