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Hydrochloric Acid → 2-(Pyridin-4-yl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine Hydrochloride

HRID 2388719
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HRID 2388719 반응식
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[S:8][C:9]3[CH2:10][N:11](C(OCC)=O)[CH2:12][CH2:13][C:14]=3[N:15]=2)=[CH:3][CH:2]=1.[OH-].[K+].[ClH:23]>>[ClH:23].[N:1]1[CH:6]=[CH:5][C:4]([C:7]2[S:8][C:9]3[CH2:10][NH:11][CH2:12][CH2:13][C:14]=3[N:15]=2)=[CH:3][CH:2]=1
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참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 68644063Ethyl 2-(pyridin-4-yl)-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate

생성물 1

HCID 686439822-(Pyridin-4-yl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine Hydrochloride수율 30%

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온도
0 °C

실험 절차

A solution of ethyl 2-(pyridin-4-yl)-6,7-dihydrothiazolo[5,4-c]pyridine-5(4H)-carboxylate (1.8 mmol) in a 3.5 N potassium hydroxide solution (3 ml) was heated under reflux for 3 hours. The course of the reaction was monitored by thin layer chromatography. The reaction mixture was then cooled to 0° C. and acidified with concentrated hydrochloric acid. The solid which had precipitated was filtered out and dried. The product was obtained in the form of the HCl salt. The yield was 30%.

후처리

  1. temperatureunder reflux for 3 hours
  2. customThe solid which had precipitated
  3. filtrationwas filtered out
  4. customdried

출처 및 근거

ORD 기록
ord-836871a3c7b54f76815c6e318de4d437
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08268814B2

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