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Hydrochloric Acid → 2-Methyl-1-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine hydrochloride

HRID 2263050
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HRID 2263050 반응식
[CH3:1][CH:2]1[N:7]([C:8]2[S:12][N:11]=[C:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[N:9]=2)[CH2:6][CH2:5][N:4](C(OC(C)(C)C)=O)[CH2:3]1.[ClH:26]>CO>[ClH:26].[CH3:1][CH:2]1[CH2:3][NH:4][CH2:5][CH2:6][N:7]1[C:8]1[S:12][N:11]=[C:10]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 68777842Tert-butyl 3-methyl-4-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxylate

생성물 1

HCID 687774352-Methyl-1-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine hydrochloride수율 82.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To tert-butyl 3-methyl-4-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxylate (6.70 g, 18.6 mmol) was added a solution of 2N hydrogen chloride in methanol (400 ml) and the mixture was stirred at room temperature for 12 hours, and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of ether and methanol to obtain the desired product (4.54 g, 82.2%) as a solid.

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후처리

  1. distillationthe solvent was distilled off under reduced pressure
  2. customThe residue was recrystallized from a mixed solvent of ether and methanol

출처 및 근거

ORD 기록
ord-dc7c4b34392749c6ba74b82714d7a984
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07851473B2

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