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Dimethylformamide dimethyl acetal → (2e)-1-(1-Acetyl-2,3-dihydro-1h-indol-5-yl)-3-(dimethylamino)prop-2-en-1-one

HRID 1510239
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HRID 1510239 반응식
[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].CO[CH:18](OC)[N:19]([CH3:21])[CH3:20]>>[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])/[CH:14]=[CH:18]/[N:19]([CH3:21])[CH3:20])=[CH:10][CH:11]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 32808501,5-Diacetylindoline

생성물 1

HCID 69081893(2e)-1-(1-Acetyl-2,3-dihydro-1h-indol-5-yl)-3-(dimethylamino)prop-2-en-1-one수율 97%

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온도
110 °C

실험 절차

A mixture of 1-(1-acetyl-2,3-dihydro-1H-indol-5-yl)ethanone (6.0 g) and N,N-dimethylformamide dimethylacetal (14.2 g) was refluxed at 110° C. for 4 hours and evaporated in vacuo. The residue was triturated with diisopropylether, collected by filtration, and dried in vacuo to afford crude (2E)-1-(1-acetyl-2,3-dihydro-1H-indol-5-yl)-3-(dimethylamino)prop-2-en-1-one (7.4 g). To a solution of crude product in methanol (100 mL) were added guanidine hydrochloride (3.56 g) and potassium tert-butoxide (3.86 g) and the mixture was stirred at 100° C. for 3 hours.

후처리

  1. customevaporated in vacuo
  2. customThe residue was triturated with diisopropylether
  3. filtrationcollected by filtration
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-d8d0e88410084b32bc70e927126b07f1
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08211919B2

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