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Buspirone Hydrochloride → Buspirone

HRID 1402639
Notes
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Reaction equation

HRID 1402639 reaction equation
[CH:1]1[CH:2]=[N:3][C:4]([N:7]2[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][CH2:15][CH2:16][N:17]3[C:27](=[O:28])[CH2:26][C:21]4([CH2:25][CH2:24][CH2:23][CH2:22]4)[CH2:20][C:18]3=[O:19])[CH2:9][CH2:8]2)=[N:5][CH:6]=1.Cl>CCO>[CH:1]1[CH:6]=[N:5][C:4]([N:7]2[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][CH2:15][CH2:16][N:17]3[C:27](=[O:28])[CH2:26][C:21]4([CH2:22][CH2:23][CH2:24][CH2:25]4)[CH2:20][C:18]3=[O:19])[CH2:9][CH2:8]2)=[N:3][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 36431Buspirone Hydrochloride

Product 1

HCID 2477Buspirone

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

0.2 grams of Phospholipin 90 were dissolved in 2.5 grams EtOH; to this solution 0.02 grams of Vitamin E were added and mixed to obtain a clear system. To this system, 0.2 grams of buspirone HCl dissolved in 7.08 grams DDW were slowly added under constant stirring at room temperature in Heidolph mixer (700 rpm). The obtained system was stirred for additional 5 minutes.

Workup

  1. additionmixed
  2. customto obtain a clear system
  3. additionwere slowly added
  4. stirringThe obtained system was stirred for additional 5 minutes

Sources & evidence

ORD record
ord-bf8638285ae54532a2da69bf1f4e4edb
Source dataset
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08911751B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes