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Hydrochloric Acid → 2-Amino-1-benzooxazol-2-yl-butan-1-one hydrochloride

HRID 1830161
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반응식

HRID 1830161 반응식
[ClH:1].C(OC(=O)[NH:8][CH:9]([C:12]([C:14]1[O:15][C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[N:18]=1)=[O:13])[CH2:10][CH3:11])(C)(C)C>O1CCOCC1.C(Cl)Cl>[ClH:1].[NH2:8][CH:9]([CH2:10][CH3:11])[C:12]([C:14]1[O:15][C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[N:18]=1)=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 58826759[1-(Benzooxazole-2-carbonyl)-propyl]-carbamic acid tert-butyl ester

생성물 1

HCID 220539252-Amino-1-benzooxazol-2-yl-butan-1-one hydrochloride

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 312751,4-Dioxane용매

실험 절차

Hydrogen chloride in dioxane (1M, 1 ml) was added to a solution of, 1-(Benzooxazole-2-carbonyl)-propyl]-carbamic acid tert-butyl ester (2a) in dry methylene chloride (3 ml) and stirred at room temperature for 4 hrs. Concentration under reduced pressure gave the title compound as white solid (65 mg); 1H NMR (CDCl3) δ 0.99 (t, J=7.5 Hz, 3H), 2.20–2.05 (m, 2H), 4.96 (m, 1H), 7.58 (t, J=7.4 Hz, 1H), 7.69 (t, J=7.4 Hz, 1H), 7.94 (d, J=8.2 Hz, 1H), 8.04 (d, J=8.2 Hz, 1H), 8.75 (m, 3H); MS: 207(MH+).

후처리

  1. concentrationConcentration under reduced pressure

출처 및 근거

ORD 기록
ord-b5a7b47ac9b64da3aa4a6ab493f808f7
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07064123B1

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