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Hydrochloric Acid → 2-(6-Aminopyridin-2-yl)-2-methoxyiminoacetic acid hydrochloride

HRID 1075252
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인쇄 미리보기

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HRID 1075252 반응식
C([NH:3][C:4]1[N:9]=[C:8]([C:10](=[N:14][O:15][CH3:16])[C:11]([OH:13])=[O:12])[CH:7]=[CH:6][CH:5]=1)=O.[ClH:17]>CO>[ClH:17].[NH2:3][C:4]1[N:9]=[C:8]([C:10](=[N:14][O:15][CH3:16])[C:11]([OH:13])=[O:12])[CH:7]=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 543262512-(6-Formamidopyridin-2-yl)-2-methoxyiminoacetic acid

생성물 1

HCID 867377252-(6-Aminopyridin-2-yl)-2-methoxyiminoacetic acid hydrochloride수율 104.7%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A suspension of 2(6-formamidopyridin-2-yl)-2-methoxyiminoacetic acid (1.5 g.) and conc. hydrochloric acid (0.77 g.) in methanol (30 ml.) was stirred at room temperature for 45 minutes. After concentrating the resultant solution under reduced pressure, the residue was washed with diethyl ether. The precipitates were collected by filtration to give 2-(6-aminopyridin-2-yl)-2-methoxyiminoacetic acid hydrochloride (1.63 g.), mp 100° to 105° C.

후처리

  1. concentrationAfter concentrating the resultant solution under reduced pressure
  2. washthe residue was washed with diethyl ether
  3. filtrationThe precipitates were collected by filtration

출처 및 근거

ORD 기록
ord-fb49c4038cc84b3b9517fe084dec4922
출처 데이터셋
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04395411

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