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Hydrochloric Acid → 3-(Hydroxyaminocarbonyl)methylimidazo[5,1-b]thiazole

HRID 1603493
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HRID 1603493 반응식
C([O:3][C:4]([CH2:6][C:7]1[N:8]2[CH:14]=[N:13][CH:12]=[C:9]2[S:10][CH:11]=1)=O)C.Cl.[NH2:16][OH:17].[O-]CC.[Na+].Cl>C(O)C>[OH:17][NH:16][C:4]([CH2:6][C:7]1[N:8]2[CH:14]=[N:13][CH:12]=[C:9]2[S:10][CH:11]=1)=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 443297Hydroxyamine hydrochlorideHCID 2723922Sodium ethoxideHCID 196050653-Ethoxycarbonylmethylimidazo[5,1-b]thiazole

생성물 1

HCID 196050273-(Hydroxyaminocarbonyl)methylimidazo[5,1-b]thiazole수율 73.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To 2 ml of an ethanol solution containing 204.3 mg of 3-ethoxycarbonylmethylimidazo[5,1-b]thiazole, 108.2 mg of hydroxylamine hydrochloride and 210.2 mg of a sodium ethoxide powder were added, and the mixture was then stirred at room temperature for 2 hours. Under ice-cooling, 0.4 ml of 1N hydrochloric acid was added to the reaction solution to neutralize the solution. The solvent was evaporated under reduced pressure, and the resulting residue was purified by Diaion HP-20 Resin to obtain 140 mg of the title compound.

후처리

  1. additionwere added
  2. temperatureUnder ice-cooling
  3. customThe solvent was evaporated under reduced pressure
  4. customthe resulting residue was purified by Diaion HP-20 Resin

출처 및 근거

ORD 기록
ord-e4a0e5b1563f4d25a1527d34a8765996
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05990101

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