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2,4,6-Trimethylpyridine → HCID 19906396, 화합물

HRID 2371790
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HRID 2371790 반응식
Br[CH:2]1[CH2:11][CH2:10][C:9]2[C:4](=[CH:5][C:6]([NH:12][C:13](=[O:20])[CH2:14][CH:15]3[CH2:19][CH2:18][CH2:17][CH2:16]3)=[CH:7][CH:8]=2)[C:3]1=[O:21].N1C(C)=CC(C)=CC=1C>O1CCCC1>[CH:15]1([CH2:14][C:13]([NH:12][C:6]2[CH:5]=[C:4]3[C:9]([CH:10]=[CH:11][CH:2]=[C:3]3[OH:21])=[CH:8][CH:7]=2)=[O:20])[CH2:19][CH2:18][CH2:17][CH2:16]1
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참가 물질

4

반응물 2

HCID 79532,4,6-TrimethylpyridineHCID 19906403HCID 19906403, 화합물

생성물 1

HCID 19906396HCID 19906396, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
160 °C

실험 절차

A mixture of 2-bromo-7-cyclopentylacetamido-1-tetralone (1.1 g) and collidine (12 ml) was heated at 160° C. for 2 h. After cooling, the reaction mixture was diluted with 1:9 tetrahydrofuran:ethyl acetate, washed (1N HCl (4 times), brine), dried (MgSO4) and evaporated to give 7-cyclopentylacetamido-1-napthol (quantitative) as a brown glassy solid which was used without further purification.

후처리

  1. temperatureAfter cooling
  2. washethyl acetate, washed (1N HCl (4 times), brine)
  3. dry with materialdried (MgSO4)
  4. customevaporated

출처 및 근거

ORD 기록
ord-af575ad36742488fb009b42953605017
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05095038

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