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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648977Generated: October 30, 2026

1-Bromo-2-methylpropane → HCID 13649199, compound

https://huagongshe.com/reaction/648977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-methylpropaneHCID 6555—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13649192HCID 13649192—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
ProductHCID 13649199HCID 1364919932.5%

Reaction Steps

5-(1-Piperazinylcarbonyl)oxindol hydrochloride (1.0 g), 1.2 g of DBU, and 0.73 g of isobutyl bromide were suspended in 15 ml of acetonitrile and the suspension was reflexed for 6 hours. To the mixture were then added 0.6 ml of triethylamine and 0.73 g of isobutyl bromide and the mixture was further reflexed for 8 hours. The reaction mixture was poured into a saturated aqueous solution of sodium hydrogencarbonate and extracted with chloroform. The chloroform layer was washed with a saturated saline solution and dried over sodium sulfate. The residue obtained after the solvent was distilled off was purified by silica-gel column chromatography (eluent: dichloromethane:methanol=20:1). The product was converted into the hydrochloride with acetone and hydrochloricacid, and recrystallized from a mixture of ethanol and methanol to give 0.39 g of 5-(4-isobutyl-1-piperazinylcarbonyl)oxindol hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04737501
Source datasetuspto-grants-1988_04
ORD IDord-dc1fbef8014e4758991aea2bebd39d34
Source noteuspto-grants-1988_04