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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36950Generated: October 28, 2026

1-Phenylpiperazine → HCID 131719006, compound

https://huagongshe.com/reaction/36950

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant3-(4-Chlorobutyl)-5-indolylureaHCID 15067402—
SolventAcetonitrileHCID 6342—
ProductHCID 131719006HCID 131719006—

Reaction Steps

A solution of 2.6 g of 3-(4-chlorobutyl)-5-indolylurea [obtainable by reacting 5-nitroindole with 4-chlorobutyryl chloride to give 3-(4-chlorobutyryl)-5nitroindole, reduction with diborane to give 3-(4-chlorobutyl)-5-nitroindole hydrogenation to 3-(4-chlorobutyl)-5-aminoindole and reaction with KCNO] and 16.3 g of 1-phenylpiperazine in ("A") in 200 ml of acetonitrile is stirred for 12 hours at 20° and worked up in a conventional manner to give 3-[4-(4-phenylpiperazino)butyl]-5-indolylurea, hydrochloride, m.p. 207° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05418237
Source datasetuspto-grants-1995_05
ORD IDord-964170a8707043ce97316fe0269f0520
Source noteuspto-grants-1995_05