HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378733Generated: October 30, 2026
4-Bromobenzyl alcohol → HCID 22013084, compound
https://huagongshe.com/reaction/378733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 15458211 | HCID 15458211 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 22013084 | HCID 22013084 | 48% |
Reaction Steps
In 10 ml of dimethyl sulfoxide was dissolved 0.336 g of (+)-1-(2,2-diethoxyethyl)-3-hydroxycarbonylmethyl-3-(N'-(4-methylphenyl)ureido)indolin-2-one. To the solution were added successively 0.108 g of 4-dimethylaminopyridine, 0.170 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and 0.166 g of 4-bromobenzyl alcohol. The resulting mixture was stirred for 18 hours, followed by concentration. The concentrate was diluted with ethyl ether, washed successively with dilute hydrochloric acid and a saturated aqueous solution of sodium hydrogencarbonate. The organic layer was dried over anhydrous sodium sulfate, and concentrated. The crude product was purified by silica gel column chromatography (hexane/ethyl acetate=2/1) to give 0.219 g (48%) of the title compound as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06031111 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-50c99c51fcef4b868bd1ab00aea8febc |
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| Source note | uspto-grants-2000_02 |
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