HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635211Generated: October 29, 2026
Diisopropylethylamine → HCID 15512221, compound
https://huagongshe.com/reaction/635211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15512220 | HCID 15512220 | — |
| Reactant | 155628-04-9 | HCID 21258207 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | HCID 15512221 | HCID 15512221 | 60.7% |
Reaction Steps
4-(4-Phenyl-1,2,3,6-tetrahydropyridin-1-yl)-2-chloro-6-methylpyrimidine (466 mg), 408 mg of 2-bromo-4-isopropylaniline hydrochloride and 232 mg of diisopropylethylamine were heated in 5 ml of ethylene glycol under reflux for 1 hour. The reaction solution was poured into a saturated aqueous solution of sodium hydrogencarbonate and extracted with ethyl acetate. The extract was washed successively with water and a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The desiccant was filtered off, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=6/1) to give 458 mg of 2-[N-(2-bromo-4-isopropylphenyl)amino]-4-(4-phenyl-1,2,3,6-tetrahydropyridin-1-yl)-6-methylpyrimidine as an amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187781B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-1b6ea8cf99c54d7d8e87e4dd255c3186 |
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| Source note | uspto-grants-2001_02 |
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