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Hydrochloric Acid → 5-(3-Aminothiophen-2-yl)-3H-[1,3,4]oxadiazol-2-one hydrochloride

HRID 460315
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인쇄 미리보기

반응식

HRID 460315 반응식
[O:1]=[C:2]1[O:6][C:5]([C:7]2[S:8][CH:9]=[CH:10][C:11]=2[NH:12]C(=O)OC(C)(C)C)=[N:4][NH:3]1.[ClH:20]>O1CCOCC1>[ClH:20].[NH2:12][C:11]1[CH:10]=[CH:9][S:8][C:7]=1[C:5]1[O:6][C:2](=[O:1])[NH:3][N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86760474tert-Butyl [2-(5-oxo-4,5-dihydro[1,3,4]oxadiazol-2-yl)thiophen-3-yl]carbamate

생성물 1

HCID 184459475-(3-Aminothiophen-2-yl)-3H-[1,3,4]oxadiazol-2-one hydrochloride

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

The mixture consisting of 100 mg of tert-butyl [2-(5-oxo-4,5-dihydro[1,3,4]oxadiazol-2-yl)thiophen-3-yl]carbamate and 5 ml of a 4 molar HCl solution in dioxane is stirred for one hour. Afterwards, the volatile fractions are removed under reduced pressure and the residue is stirred with 5 ml of tert-butyl methyl ether and the product is filtered off with suction and dried under reduced pressure.

후처리

  1. customAfterwards, the volatile fractions are removed under reduced pressure
  2. stirringthe residue is stirred with 5 ml of tert-butyl methyl ether
  3. filtrationthe product is filtered off with suction
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-8475ffae7edb463ca082a53f4072f3bc
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07196114B2

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