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Ethanolamine → 2-(4-Pyridine-2-ylbenzoylamino)ethanol

HRID 1860108
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HRID 1860108 반응식
C(N(CC)CC)C.Cl.[N:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]1[CH:23]=[CH:22][C:18]([C:19](Cl)=[O:20])=[CH:17][CH:16]=1.[CH2:24]([CH2:26][NH2:27])[OH:25]>ClCCl>[N:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]1[CH:23]=[CH:22][C:18]([C:19]([NH:27][CH2:26][CH2:24][OH:25])=[O:20])=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 700EthanolamineHCID 8471TriethylamineHCID 186259104-(2-Pyridinyl)benzoyl Chloride Hydrochloride

생성물 1

HCID 186260452-(4-Pyridine-2-ylbenzoylamino)ethanol

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Triethylamine (0.14 ml) was added to a suspension of 4-pyridine-2-ylbenzoylchloride hydrochloride (254 mg) in dichloromethane (2 ml). To the mixture a solution of ethanolamine (0.060 ml) in dichloromethane (3 ml) was added. This mixture was stirred for 30 minutes. At the end of this time the reaction mixture was concentrated and the residue was partitioned between ethyl acetate and water. The ethyl acetate layer was separated and washed with aqueous sodium chloride and dried over anhydrous magnesium sulfate and concentrated to afford crystals. The crystals were washed with isopropyl ether to afford the title compound (111 mg).

후처리

  1. concentrationAt the end of this time the reaction mixture was concentrated
  2. customthe residue was partitioned between ethyl acetate and water
  3. customThe ethyl acetate layer was separated
  4. washwashed with aqueous sodium chloride
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated
  7. customto afford crystals
  8. washThe crystals were washed with isopropyl ether

출처 및 근거

ORD 기록
ord-c153b5dbf4ee48728e46e47f9136b404
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06528525B1

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