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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13649192 | HCID 13649192 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 13649199 | HCID 13649199 | 32.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04737501 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-dc1fbef8014e4758991aea2bebd39d34 |
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| Source note | uspto-grants-1988_04 |
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