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N-(2-{2-[3-(benzyloxy)butyl]-7,8-dihydro-6H-indeno[5,4-d][1,3]oxazol-8-yl}ethyl)acetamide → N-{2-[2-(3-Hydroxybutyl)-7,8-dihydro-6H-indeno[5,4-d][1,3]oxazol-8-yl]ethyl}acetamide

HRID 340719
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인쇄 미리보기

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HRID 340719 반응식
C([O:8][CH:9]([CH3:30])[CH2:10][CH2:11][C:12]1[O:13][C:14]2[C:23]3[CH:22]([CH2:24][CH2:25][NH:26][C:27](=[O:29])[CH3:28])[CH2:21][CH2:20][C:19]=3[CH:18]=[CH:17][C:15]=2[N:16]=1)C1C=CC=CC=1>CO.[C].[Pd]>[OH:8][CH:9]([CH3:30])[CH2:10][CH2:11][C:12]1[O:13][C:14]2[C:23]3[CH:22]([CH2:24][CH2:25][NH:26][C:27](=[O:29])[CH3:28])[CH2:21][CH2:20][C:19]=3[CH:18]=[CH:17][C:15]=2[N:16]=1
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참가 물질

4

반응물 1

HCID 57781203N-(2-{2-[3-(benzyloxy)butyl]-7,8-dihydro-6H-indeno[5,4-d][1,3]oxazol-8-yl}ethyl)acetamide

생성물 1

HCID 57781241N-{2-[2-(3-Hydroxybutyl)-7,8-dihydro-6H-indeno[5,4-d][1,3]oxazol-8-yl]ethyl}acetamide수율 84%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 887Methanol용매

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온도
50 °C

실험 절차

To a solution of N-(2-{2-[3-(benzyloxy)butyl]-7,8-dihydro-6H-indeno[5,4-d][1,3]oxazol-8-yl}ethyl)acetamide (155 mg, 0.381 mmol) in methanol (4 mL) was added a 10% palladium-carbon powder (300 mg), and the mixture was stirred at 50° C. for 4 hr under a hydrogen atmosphere. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methanol/ethyl acetate=0/100→5/95) to give the title compound (101 mg, yield 84%).

후처리

  1. filtrationThe catalyst was filtered off
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customThe residue was purified by silica gel column chromatography (methanol/ethyl acetate=0/100→5/95)

출처 및 근거

ORD 기록
ord-813f83e821c94caca3c6f424ccf0b874
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895591B2

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