HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182065Generated: October 31, 2026
Diisopropylethylamine → HCID 12069440, compound
https://huagongshe.com/reaction/2182065
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 12069439 | HCID 12069439 | — |
| Reactant | HCID 22482749 | HCID 22482749 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12069440 | HCID 12069440 | 26.7% |
Reaction Steps
In 4 ml of ethanol, 0.27 g of 5-carbamoyl-1,2,3,6-tetrahydropyridine trifluoroacetate and 0.36 g of 4-chloro-7-(4-isopropyl-2-methylthiophenyl)-2,5,6-trimethyl-7H-pyrrolo[2,3-d]pyrimidine were dissolved, and subsequently, 0.39 g of diisopropylethylamine was added thereto. The reaction mixture was heated under reflux for 8.5 hours, and subsequently, a saturated aqueous solution of sodium hydrogencarbonate was poured thereinto. The reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and was then dried over anhydrous sodium sulfate. After the desiccant was filtered off, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: chloroform-methanol=60:1), followed by crystallization from a mixed solvent of ethyl acetate-diethyl ether to yield 0.12 g of 4-(5-carbamoyl-1,2,3,6-tetrahydropyridin-1-yl)-7-(4-isopropyl-2-methylthiophenyl)-2,5,6-trimethyl-7H-pyrrolo[2,3-d]pyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06894168B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-6dce93b320e1489e882b3bbcd1219c8f |
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| Source note | uspto-grants-2005_05 |
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