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Hydrochloric Acid → HCID 86670327, 화합물

HRID 1972426
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HRID 1972426 반응식
[ClH:1].[CH2:2]([C@@H:4]1[N:9]([C:10]2[CH:15]=[CH:14][C:13]([C:16]([OH:25])([C:21]([F:24])([F:23])[F:22])[C:17]([F:20])([F:19])[F:18])=[CH:12][CH:11]=2)[CH2:8][CH2:7][N:6](C(OC(C)(C)C)=O)[CH2:5]1)[CH3:3]>C(Cl)Cl>[ClH:1].[CH2:2]([C@H:4]1[CH2:5][NH:6][CH2:7][CH2:8][N:9]1[C:10]1[CH:15]=[CH:14][C:13]([C:16]([OH:25])([C:17]([F:19])([F:20])[F:18])[C:21]([F:22])([F:23])[F:24])=[CH:12][CH:11]=1)[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86670326HCID 86670326, 화합물

생성물 1

HCID 86670327HCID 86670327, 화합물수율 87.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

HCl (4.0 M solution with 1,4-dioxane, 3.9 mL, 16 mmol) was added to a stirring solution of tert-butyl (3S)-3-ethyl-4-(4-(2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl)phenyl)-1-piperazinecarboxylate (0.71 g, 1.6 mmol) and CH2Cl2 (7.8 mL) at room temperature. After 18 h, the reaction mixture was concentrated to give 2-(4-((2S)-2-ethyl-1-piperazinyl)phenyl)-1,1,1,3,3,3-hexafluoro-2-propanol hydrochloride (0.55 g) as a brown solid. The material was used in the next step without purification.

후처리

  1. concentrationthe reaction mixture was concentrated

출처 및 근거

ORD 기록
ord-cc780871c63d4f4b8399d1948cca1b1c
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431563B2

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