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Hydrochloric Acid → HCID 12952783, compound

HRID 1263247
Notes
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Reaction equation

HRID 1263247 reaction equation
[CH3:1][O:2][CH:3](OC)[CH2:4][NH:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=2)[CH2:10][CH2:9]1)=[S:7].Cl.C(=O)([O-])O.[Na+]>>[CH3:1][O:2][CH:3]1[S:7][C:6]([N:8]2[CH2:13][CH2:12][N:11]([C:14]3[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=3)[CH2:10][CH2:9]2)=[N:5][CH2:4]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 12952797HCID 12952797, compound

Product 1

HCID 12952783HCID 12952783, compoundYield 73%

Procedure

A mixture of 6 parts of N-(2,2-dimethoxyethyl)-4-(4-hydroxyphenyl)-1-piperazinecarbothioamide and 25 parts of a diluted hydrochloric acid solution is stirred overnight at room temperature. Upon the addition of sodium hydrogen carbonate, the product is allowed to crystallize. It is filtered off and recrystallized from ethanol, yielding 4.3 parts (73%) of 4-[4-(4,5-dihydro-5-methoxy-2-thiazolyl)-1-piperazinyl]phenol; mp. 165.6° C.

Workup

  • customto crystallize
  • filtrationIt is filtered off
  • customrecrystallized from ethanol
  • Sources & evidence

    ORD record
    ord-2b635828b7b2460d9a5882c023b12102
    Source dataset
    uspto-grants-1984_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04456605

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes