HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226397Generated: October 26, 2026
Triethylamine → ethyl (2E)-3-(5-{[(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-2-pyrazinyl)acrylate
https://huagongshe.com/reaction/226397
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3R)-1-(4-chlorobenzoyl)-3-pyrrolidinamine | HCID 68963176 | — |
| Reactant | Ethyl (2E)-3-(5-chloro-2-pyrazinyl)acrylate | HCID 86603667 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl (2E)-3-(5-{[(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-2-pyrazinyl)acrylate | HCID 86603707 | 63.8% |
Reaction Steps
To a solution of ethyl (2E)-3-(5-chloro-2-pyrazinyl)acrylate (500 mg) in DMF (5 mL) was added (3R)-1-(4-chlorobenzoyl)-3-pyrrolidinamine (951 mg) and Et3N (1.15 mL). After stirring for 3 hours at 120° C., the reaction mixture was partitioned between ethyl acetate and H2O. The organic layer was washed with H2O, dried over MgSO4, filtered, and evaporated in vacuo. The residue was purified by column chromatography on silica gel to give ethyl (2E)-3-(5-{[(3R)-1-(4-chlorobenzoyl)-3-pyrrolidinyl]amino}-2-pyrazinyl)acrylate (601 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557127B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-f57b190b038a4c4c84adc18698a2f268 |
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| Source note | uspto-grants-2009_07 |
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