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Hydrochloric Acid → 1-[5-(1H-Pyrazol-4-yl)-pyridin-2-yl]-cyclobutylamine dihydrochloride

HRID 2038759
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반응식

HRID 2038759 반응식
C(OC(=O)[NH:7][C:8]1([C:12]2[CH:17]=[CH:16][C:15]([C:18]3[CH:19]=[N:20][NH:21][CH:22]=3)=[CH:14][N:13]=2)[CH2:11][CH2:10][CH2:9]1)(C)(C)C.C(O)(C(F)(F)F)=O.[ClH:31].O1CCOCC1>C(Cl)Cl>[ClH:31].[ClH:31].[NH:20]1[CH:19]=[C:18]([C:15]2[CH:16]=[CH:17][C:12]([C:8]3([NH2:7])[CH2:11][CH2:10][CH2:9]3)=[N:13][CH:14]=2)[CH:22]=[N:21]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 6422Trifluoroacetic acidHCID 312751,4-DioxaneHCID 68379199{1-[5-(1H-pyrazol-4-yl)-pyridin-2-yl]-cyclobutyl}-carbamic acid tert-butyl ester

생성물 1

HCID 683790391-[5-(1H-Pyrazol-4-yl)-pyridin-2-yl]-cyclobutylamine dihydrochloride

시약·촉매·용매 1

HCID 6344
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
Dichloromethane
용매

실험 절차

To a solution of {1-[5-(1H-pyrazol-4-yl)-pyridin-2-yl]-cyclobutyl}-carbamic acid tert-butyl ester (300 mg, 0.96 mmol) in CH2Cl2 (5 mL) was added TFA (0.37 mL, 4.8 mmol). After 15 h, 4M HCl in dioxane (1.2 mL, 4.8 mmol) was added. After 1 h, the reaction was concentrated in-vacuo to yield 303 mg of the title compound, m/z 215.4 [M+H]+.

후처리

  1. waitAfter 1 h
  2. concentrationthe reaction was concentrated in-vacuo

출처 및 근거

ORD 기록
ord-ab8fb77e4c8e4faca721c2c16f191b1d
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08575360B2

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