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Hydrochloric Acid → N-[3-(Piperidin-4-ylamino)-phenyl]-acetamide dihydrochloride

HRID 2355539
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인쇄 미리보기

반응식

HRID 2355539 반응식
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([NH:21][C:22](=[O:24])[CH3:23])[CH:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:25]>O1CCOCC1>[ClH:25].[ClH:25].[NH:8]1[CH2:9][CH2:10][CH:11]([NH:14][C:15]2[CH:16]=[C:17]([NH:21][C:22](=[O:24])[CH3:23])[CH:18]=[CH:19][CH:20]=2)[CH2:12][CH2:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 674007394-(3-Acetylamino-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 67400427N-[3-(Piperidin-4-ylamino)-phenyl]-acetamide dihydrochloride

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A solution of 4-(3-acetylamino-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (0.21 g, 0.63 mmol) in 4 M HCl in dioxane (10 mL) was stirred at rt for 2 h. The solvent was removed under reduced pressure and the crude product used in the consecutive step without further purification assuming quantitative deprotection and formation of the dihydrochloride salt. MS (ISP): 234.4 [M+H]+.

후처리

  1. customThe solvent was removed under reduced pressure
  2. customthe crude product used in the consecutive step without further purification

출처 및 근거

ORD 기록
ord-ec0edd25e33c4adc9d98a34ce06cca0d
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07754744B2

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