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Triethylamine → 3-Chloro-benzofuro[3,2-c]isoquinoline-5-ol

HRID 869425
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반응식

HRID 869425 반응식
COC(=O)[CH:4]([C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[CH:8][C:7]=1[C:13](OC)=[O:14])Br.[OH:18][C:19]1[CH:26]=[CH:25][CH:24]=[CH:23][C:20]=1[C:21]#[N:22].C(N(CC)CC)C>CC#N>[Cl:12][C:9]1[CH:8]=[C:7]2[C:6]([C:4]3[O:18][C:19]4[CH:26]=[CH:25][CH:24]=[CH:23][C:20]=4[C:21]=3[N:22]=[C:13]2[OH:14])=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 119072-HydroxybenzonitrileHCID 867222712-(4-Chloro-2-methoxycarbonyl-phenyl)-2-bromo-acetic acid methyl ester

생성물 1

HCID 1785169623-Chloro-benzofuro[3,2-c]isoquinoline-5-ol수율 56.7%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of 19A (crude, 20.29 mmol) and 2-hydroxy-benzonitrile (20.29 mmol) in MeCN (100 mL) was stirred at room temperature. To the solution was added triethylamine (TEA, 20.44 g, 202.9 mmol) dropwise. After addition completed, the reaction was refluxed for 24 hours, then cooled. The precipitated solids were collected by filtration, washed with a small amount of MeCN, then washed with water several times until there was no TEA salt, dried to give pure product 19B (3.1 g).

후처리

  1. additionAfter addition
  2. temperaturethe reaction was refluxed for 24 hours
  3. temperaturecooled
  4. filtrationThe precipitated solids were collected by filtration
  5. washwashed with a small amount of MeCN
  6. washwashed with water several times until there
  7. customdried

출처 및 근거

ORD 기록
ord-e40dfa1c9ea24f92b74a4bff7a070602
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969373B2

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