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1-(2-Methoxyphenyl)piperazine → 8-((3-(4-(2-Methoxyphenyl)piperazin-1-yl)-2-hydroxypropyl)oxy)thiochroman

HRID 1729222
Notes
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Reaction equation

HRID 1729222 reaction equation
[O:1]1[CH2:15][CH:2]1[CH2:3][O:4][C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:14]=1[S:13][CH2:12][CH2:11][CH2:10]2.[CH3:16][O:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[N:24]1[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]1>O1CCCC1>[CH3:16][O:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[N:24]1[CH2:29][CH2:28][N:27]([CH2:15][CH:2]([OH:1])[CH2:3][O:4][C:5]2[CH:6]=[CH:7][CH:8]=[C:9]3[C:14]=2[S:13][CH2:12][CH2:11][CH2:10]3)[CH2:26][CH2:25]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 13461-(2-Methoxyphenyl)piperazineHCID 158404152-{[(3,4-Dihydro-2H-1-benzothiopyran-8-yl)oxy]methyl}oxirane

Product 1

HCID 30739008-((3-(4-(2-Methoxyphenyl)piperazin-1-yl)-2-hydroxypropyl)oxy)thiochroman

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

140 mg (0.63 mmol) of the compound obtained in Step A are dissolved in 1.5 cm3 of anhydrous tetrahydrofuran. 600 mg (3.15 mmol) of 1-(2-methoxyphenyl)piperazine, diluted in 1.5 cm3 of anhydrous tetrahydrofuran, are added.

Workup

  1. additionare added

Sources & evidence

ORD record
ord-448ea7be745046d1a0a3d42e3378b2f4
Source dataset
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05332741

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes