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Hydrochloric Acid → 5-Chlorothiazolo[5,4-b]pyridin-2(1H)-one

HRID 1845901
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HRID 1845901 반응식
[Cl:1][C:2]1[N:7]=[C:6]2[S:8][C:9]([O:11]C)=[N:10][C:5]2=[CH:4][CH:3]=1.O1CCOCC1.Cl>O>[Cl:1][C:2]1[N:7]=[C:6]2[S:8][C:9](=[O:11])[NH:10][C:5]2=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 772309095-Chloro-2-methoxy[1,3]thiazolo[5,4-b]pyridine

생성물 1

HCID 144231285-Chlorothiazolo[5,4-b]pyridin-2(1H)-one

시약·촉매·용매 1

HCID 962Water용매2회

반응 조건

온도
95 °C

실험 절차

To round bottom flask was added give 5-chloro-2-methoxy[1,3]thiazolo[5,4-b]pyridine (1-3) (5.76 g, 28.7 mmol), 1,4-dioxane (90 mL), and a 6N solution of HCl in water (23.9 mL, 144 mmol). The reaction mixture was then heated to 95° C. while stirring in a hot oil bath with a water cooled reflux condenser attached under an atmosphere of nitrogen for 20 minutes. The crude reaction mixture was then allowed to cool to room temperature, diluted methanol and concentrated to give 5-chloro[1,3]thiazolo[5,4-b]pyridin-2(1H)-one (1-4) as a tan solid. HRMS (M+H)+: observed=186.9731, calculated=186.9727.

후처리

  1. additionTo round bottom flask was added
  2. temperaturecooled
  3. temperaturereflux condenser
  4. customThe crude reaction mixture
  5. temperatureto cool to room temperature
  6. concentrationdiluted methanol and concentrated

출처 및 근거

ORD 기록
ord-447eba502ec9487a979bd8372ba91c6e
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08952005B2

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