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Hydrochloric Acid → 5-Bromo-2-(4-phenethylthiazol-2-ylamino)pyridin-4-ol hydrochloride

HRID 911065
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인쇄 미리보기

반응식

HRID 911065 반응식
C([O:8][C:9]1[C:14]([Br:15])=[CH:13][N:12]=[C:11]([NH:16][C:17]2[S:18][CH:19]=[C:20]([CH2:22][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[N:21]=2)[CH:10]=1)C1C=CC=CC=1.[ClH:30]>O1CCOCC1>[ClH:30].[Br:15][C:14]1[C:9]([OH:8])=[CH:10][C:11]([NH:16][C:17]2[S:18][CH:19]=[C:20]([CH2:22][CH2:23][C:24]3[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=3)[N:21]=2)=[N:12][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric Acid2회HCID 866347774-(benzyloxy)-5-bromo-N-(4-phenethylthiazol-2-yl)pyridin-2-amine

생성물 1

HCID 1784796325-Bromo-2-(4-phenethylthiazol-2-ylamino)pyridin-4-ol hydrochloride수율 89%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
95 °C

실험 절차

A flask was charged with 4-(benzyloxy)-5-bromo-N-(4-phenethylthiazol-2-yl)pyridin-2-amine (1.0 g, 2.1 mmol), dioxane (20 mL), concentrated HCl (70 mL) and 6N HCl (10 mL). The reaction was stirred at 95° C. overnight. The reaction was filtered and the collected solids were washed with water and under high vacuum overnight to give the desired product (0.80 g, 89% yield) as light yellow solid.

후처리

  1. filtrationThe reaction was filtered
  2. washthe collected solids were washed with water and under high vacuum overnight

출처 및 근거

ORD 기록
ord-c3aa2c914a534f7ca53d19cd7f042d8a
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022222B2

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