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2-Aminophenol → HCID 1211386, 화합물

HRID 1457652
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HRID 1457652 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].C(N(CC)CC)C.Cl.[Cl:17][C:18]1[C:23]([C:24](Cl)=[O:25])=[CH:22][CH:21]=[CH:20][N:19]=1>O1CCCC1>[OH:8][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:1][C:24]([C:23]1[C:18]([Cl:17])=[N:19][CH:20]=[CH:21][CH:22]=1)=[O:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 58012-AminophenolHCID 8471TriethylamineHCID 234977532-Chloropyridine-3-carbonyl chloride hydrochloride

생성물 1

HCID 1211386HCID 1211386, 화합물수율 41.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

As described in J. Med. Chem., 37, 519 (1994), a solution of 1.09 g of 2-aminophenol in 15 ml of tetrahydrofuran is added dropwise to a mixture of 2.1 g of triethylamine and 2.33 g of 2-chloropyridine-3-carbonyl chloride hydrochloride in 10 ml of tetrahydrofuran. The mixture is stirred at room temperature for one hour under argon and then refluxed for one hour. The solvent is removed under vacuum and the residue triturated with water: The solid is filtered off and washed with water to give 1.02 g of solid. Recrystallization from 2-propanol gives crystals, m.p. 145°-146° C.

후처리

  1. temperaturerefluxed for one hour
  2. customThe solvent is removed under vacuum
  3. customthe residue triturated with water
  4. filtrationThe solid is filtered off
  5. washwashed with water

출처 및 근거

ORD 기록
ord-3c5aff55c6c74b3d97a31f910df50f0a
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05849735

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