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Hydrochloric Acid → (4-Methyl-quinolin-2-yl)-piperidin-4-yl-amine dihydrochloride

HRID 913094
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인쇄 미리보기

반응식

HRID 913094 반응식
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([NH:14][C:15]2[CH:24]=[C:23]([CH3:25])[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:16]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:26]>O1CCOCC1>[ClH:26].[ClH:26].[CH3:25][C:23]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[N:16]=[C:15]([NH:14][CH:11]2[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]2)[CH:24]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 674000874-(4-Methyl-quinolin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 67400534(4-Methyl-quinolin-2-yl)-piperidin-4-yl-amine dihydrochloride

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

A solution of 4-(4-methyl-quinolin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (0.54 g, 1.58 mmol) in 4 M HCl in dioxane (50 mL) was stirred at rt for 1 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): 242.4 [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-86f5a1bd7da64430af772439c9338a4b
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08026255B2

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