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Hydrochloric Acid → 4-(5-(4-Fluoro-phenyl)-pyridine-2-yl)-piperazine Hydrochloride

HRID 1864752
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인쇄 미리보기

반응식

HRID 1864752 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[CH:10][C:11]([N:14]3[CH2:19][CH2:18][N:17](C=O)[CH2:16][CH2:15]3)=[N:12][CH:13]=2)=[CH:4][CH:3]=1.[ClH:22]>CO>[ClH:22].[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:9]=[CH:10][C:11]([N:14]3[CH2:15][CH2:16][NH:17][CH2:18][CH2:19]3)=[N:12][CH:13]=2)=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 231334904-(5-(4-Fluoro-phenyl)-pyridine-2-yl)-piperazine-1-carbaldehyde

생성물 1

HCID 231335334-(5-(4-Fluoro-phenyl)-pyridine-2-yl)-piperazine Hydrochloride수율 100%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

4-(5-(4-Fluoro-phenyl)-pyridine-2-yl)-piperazine-1-carbaldehyde (98 mg, 0.34 mmol) was dissolved in MeOH (5 ml) and conc. HCl (12M, 5 ml) was added. The mixture was stirred at room temperature over night. The solvents were removed in vacuo and the remaining water was removed by azeotropic evaporation using EtOH/Toulene affording 102 mg (100%) of the title compound as a yellow powder.

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후처리

  1. customThe solvents were removed in vacuo
  2. customthe remaining water was removed by azeotropic evaporation

출처 및 근거

ORD 기록
ord-836a2cfc2d6940b198c340506a93c0dd
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07625934B2

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