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Hydrochloric Acid → 4-[(2-Methylimidazo(1,2-a)pyridin 3-yl)methyl]benzonitrile hydrochloride

HRID 266059
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인쇄 미리보기

반응식

HRID 266059 반응식
[CH3:1][C:2]1[N:3]=[C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][N:5]2[C:10]=1[CH2:11][C:12]1[CH:19]=[CH:18][C:15]([C:16]#[N:17])=[CH:14][CH:13]=1.C(OCC)(=O)C.[ClH:26]>C(O)C>[ClH:26].[CH3:1][C:2]1[N:3]=[C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][N:5]2[C:10]=1[CH2:11][C:12]1[CH:13]=[CH:14][C:15]([C:16]#[N:17])=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 190324654-[(2-Methylimidazo(1,2-a)pyridin3-yl)methyl]benzonitrile

생성물 1

HCID 190324644-[(2-Methylimidazo(1,2-a)pyridin 3-yl)methyl]benzonitrile hydrochloride

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 5 g of the product of Stage C, 80 ml of ethyl acetate and 3.5 ml of 6.6N hydrochloric acid in ethanol was ice-cooled, separated, washed with ethyl acetate and dried under reduced pressure at 80° C. to obtain 5 g of the expected product melting at 230° C.

후처리

  1. temperaturecooled
  2. customseparated
  3. washwashed with ethyl acetate
  4. customdried under reduced pressure at 80° C.

출처 및 근거

ORD 기록
ord-248af269534d45e8b3eb0bbc2a4a408f
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05650414

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