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Methyl 2-{4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}-6-chloroisonicotinate → Methyl 2-(4-aminopiperidin-1-yl)-6-chloroisonicotinate hydrochloride salt

HRID 2233879
노트
인쇄 미리보기

반응식

HRID 2233879 반응식
C(OC([NH:8][CH:9]1[CH2:14][CH2:13][N:12]([C:15]2[CH:16]=[C:17]([CH:22]=[C:23]([Cl:25])[N:24]=2)[C:18]([O:20][CH3:21])=[O:19])[CH2:11][CH2:10]1)=O)(C)(C)C>Cl.O1CCOCC1>[ClH:25].[NH2:8][CH:9]1[CH2:10][CH2:11][N:12]([C:15]2[CH:16]=[C:17]([CH:22]=[C:23]([Cl:25])[N:24]=2)[C:18]([O:20][CH3:21])=[O:19])[CH2:13][CH2:14]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86608242Methyl 2-{4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}-6-chloroisonicotinate2회

생성물 1

HCID 86608260Methyl 2-(4-aminopiperidin-1-yl)-6-chloroisonicotinate hydrochloride salt수율 200%

시약·촉매·용매 1

HCID 204431481,4-Dioxane hydrochloride용매

실험 절차

Methyl 2-{4-[(tert-butoxycarbonyl)amino]piperidin-1-yl}-6-chloroisonicotinate (Intermediate 23, 1.81 g, 4.9 mmol) was dissolved in 4 N HCl/dioxane (200 ml). The mixture was stirred at room temperature for 2 h. The solvent was removed under vacuum to give the title compound (1.5 g).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
custom
The solvent was removed under vacuum

출처 및 근거

ORD 기록
ord-5a28872fc9ec48b28f06254db2780570
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709503B2

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