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Hydrochloric Acid → HCID 22640745, 화합물

HRID 2415126
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HRID 2415126 반응식
C(OC(=O)[NH:7][CH2:8][CH2:9][CH2:10][NH:11][C:12]1[CH:21]=[C:20]([O:22][CH3:23])[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=1)(C)(C)C.[ClH:25]>ClCCl.O1CCOCC1>[ClH:25].[ClH:25].[CH3:23][O:22][C:20]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=[C:12]([NH:11][CH2:10][CH2:9][CH2:8][NH2:7])[CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 57437795[3-(4-Methoxyquinolin-2-ylamino)propyl]carbamic acid tert-butyl ester

생성물 1

HCID 22640745HCID 22640745, 화합물수율 99%

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 312751,4-Dioxane용매

실험 절차

A solution of [3-(4-methoxyquinolin-2-ylamino)propyl]carbamic acid tert-butyl ester (3.10 g, 9.35 mmol) in anhydrous dichloromethane (20 ml) was treated with 4N HCl in 1,4-dioxane (10 ml). It was stirred at ambient temperature for 2 hours then was evaporated under reduced pressure to give N′-(4-methoxyquinolin-2-yl)propane-1,3-diamine dihydrochloride (2.81 g, 99%) as a white solid. [M+H]+ 232.

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후처리

  1. customthen was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-8d16d3f71dd04507b92ee356ac88b29c
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06818655B2

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