HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371127Generated: October 31, 2026
Triethylamine → N-(5-tert-Butylisoxazol-3-yl)-4-{[(3S)-1-cyclopropylpiperidin-3-yl]methyl}piperazine-1-carboxamide
https://huagongshe.com/reaction/2371127
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl 5-tert-butylisoxazol-3-ylcarbamate | HCID 13489605 | — |
| Reactant | 1-{[(3S)-1-cyclopropylpiperidin-3-yl]methyl}piperazine | HCID 59846094 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ammonia | HCID 222 | — |
| Product | N-(5-tert-Butylisoxazol-3-yl)-4-{[(3S)-1-cyclopropylpiperidin-3-yl]methyl}piperazine-1-carboxamide | HCID 57656670 | 105.1% |
Reaction Steps
A mixture of 1-{[(3S)-1-cyclopropylpiperidin-3-yl]methyl}piperazine (60 mg), phenyl(5-tert-butylisoxazol-3-yl)carbamate (84 mg) and triethylamine (54 mg) in tetrahydrofuran (4 mL) was heated to 60° C. in the microwave for 1 hour. The solution was concentrated at reduced pressure and then purified by reverse phase prep HPLC eluting with a mixture of 5-95% acetonitrile in water and then SCX-2 column eluting with methanol then 7M NH3 in methanol to give the title compound as a white solid (55 mg, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710224B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-4a9bf386f88d4db5a8a0f770f9d0cacf |
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| Source note | uspto-grants-2014_04 |
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