HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668835Generated: October 31, 2026
Diisopropylethylamine → benzyl-(2-chloro-6,7-dihydro-5H-cyclopentapyrimidin-4-yl)-ethyl-amine
https://huagongshe.com/reaction/1668835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-Ethylbenzylamine | HCID 84352 | — |
| Reactant | 2,4-dichloro-5H,6H,7H-cyclopenta(d)pyrimidine | HCID 231331 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | benzyl-(2-chloro-6,7-dihydro-5H-cyclopentapyrimidin-4-yl)-ethyl-amine | HCID 59362933 | 99.3% |
Reaction Steps
A mixture of 2,4-dichloro-6,7-dihydro-5H-cyclopentapyrimidine (0.4 g, 2.1 mmol), N-benzyl-ethylamine (0.35 mL, 2.3 mmol) and diisopropylethylamine (0.4 mL, 2.1 mmol) in anhydrous ethanol (5 mL) was heated at a temperature in the range of 20° C. to 90° C. for 18 hours. After cooling to about 20 to 35° C., the reaction mixture was concentrated under reduced pressure. The crude residue was diluted with ethyl acetate, washed with water, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to afford a light pink liquid (0.60 g, 98% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989463B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-8e00028cc6cc4a17b9db62d21a41660a |
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| Source note | uspto-grants-2011_08 |
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