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Water → 1-(3-Chloropyridin-2-yl)piperidin-4-ol

HRID 404564
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HRID 404564 반응식
Cl[C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][N:3]=1.O[CH:10]1[CH2:15][NH:14][CH2:13][CH2:12][CH2:11]1.[OH2:16]>CS(C)=O>[Cl:8][C:7]1[C:2]([N:14]2[CH2:13][CH2:12][CH:11]([OH:16])[CH2:10][CH2:15]2)=[N:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 169882,3-DichloropyridineHCID 232933-Hydroxypiperidine2회

생성물 1

HCID 607016561-(3-Chloropyridin-2-yl)piperidin-4-ol

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

2,3-dichloropyridine (10 g, 68 mmol) and 5-hydroxyl piperidine (compound 19) (26 g, 272 mmol) in DMSO was heated at 120° C. and stirred overnight. After the reaction was completed, three times of water was added into the reaction solution. The reaction mixture was extracted by ethyl acetate. The organic layer was evaporated to give a crude product, which was purified using column chromatography to give the product. (17 g, 93%)

후처리

  1. extractionThe reaction mixture was extracted by ethyl acetate
  2. customThe organic layer was evaporated

출처 및 근거

ORD 기록
ord-f815850a6cf4438fa49e999c908cfc72
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08748610B2

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