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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Piperidin-4-ol → HCID 67608386, 화합물

HRID 1409718
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HRID 1409718 반응식
Br[C:2]1[CH:7]=[N:6][C:5]([CH2:8][CH3:9])=[CH:4][N:3]=1.[OH:10][CH:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1>C(O)(C)C>[CH2:8]([C:5]1[N:6]=[CH:7][C:2]([N:14]2[CH2:15][CH2:16][CH:11]([OH:10])[CH2:12][CH2:13]2)=[N:3][CH:4]=1)[CH3:9]
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참가 물질

4

반응물 2

HCID 79341Piperidin-4-olHCID 457876282-Bromo-5-ethylpyrazine

생성물 1

HCID 67608386HCID 67608386, 화합물

시약·촉매·용매 1

HCID 3776Isopropanol용매

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온도
150 °C

실험 절차

A mixture of 2-bromo-5-ethyl-pyrazine (1.66 g) and 4-hydroxy-piperidine (2.24 g) in isopropanol (15 mL) is heated in an autoclave to 150° C. over night. The solvent is evaporated in vacuo and the residue is mixed with water and dichloromethane. The aqueous phase is extracted with dichloromethane and the combined organic phases are washed with brine, dried over MgSO4, and concentrated in vacuo to give the title compound. LC (method 7): tR=0.66 min; Mass spectrum (ESI+): m/z=208 [M+H]+.

후처리

  1. customThe solvent is evaporated in vacuo
  2. additionthe residue is mixed with water and dichloromethane
  3. extractionThe aqueous phase is extracted with dichloromethane
  4. washthe combined organic phases are washed with brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-8c0cd69fc6694b87b330ad5fb6e42c0e
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921398B2

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