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3-(2-(N-tert-Butoxycarbonylamino)ethoxy)-4-(1-hydroxyisopropyl)-5-phenylisoxazole → 3-(2-Aminoethoxy)-4-isopropenyl-5-phenylisoxazole hydrochloride

HRID 612901
노트
인쇄 미리보기

반응식

HRID 612901 반응식
C(OC([NH:8][CH2:9][CH2:10][O:11][C:12]1[C:16]([C:17](O)([CH3:19])[CH3:18])=[C:15]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[O:14][N:13]=1)=O)(C)(C)C.[ClH:27].O1CCOCC1>>[ClH:27].[NH2:8][CH2:9][CH2:10][O:11][C:12]1[C:16]([C:17]([CH3:19])=[CH2:18])=[C:15]([C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[O:14][N:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 195965303-(2-(N-tert-Butoxycarbonylamino)ethoxy)-4-(1-hydroxyisopropyl)-5-phenylisoxazoleHCID 204431481,4-Dioxane hydrochloride

생성물 1

HCID 195965933-(2-Aminoethoxy)-4-isopropenyl-5-phenylisoxazole hydrochloride수율 83%

반응 조건

온도
100 °C

실험 절차

3-(2-(N-tert-Butoxycarbonylamino)ethoxy)-4-(1-hydroxyisopropyl)-5-phenylisoxazole (0.13 g) was dissolved in a 4N hydrochloric acid/1,4-dioxane solution (10 ml), and the solution was stirred at 100° C. for one hour. After the reaction, the reaction mixture was left to be cooled, followed by evaporation of the solvent under reduced pressure. The residue was washed with ethyl acetate to obtain the title compound (0.10 g, 83%) as colorless crystals.

후처리

  1. customAfter the reaction
  2. waitthe reaction mixture was left
  3. temperatureto be cooled
  4. customfollowed by evaporation of the solvent under reduced pressure
  5. washThe residue was washed with ethyl acetate

출처 및 근거

ORD 기록
ord-f493ffc7cc574ba689329d75364963ae
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06005116

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