HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384664Generated: October 25, 2026
Ethyl 2,5-dimethoxy-tetrahydrofuran-3-carboxylate → tert-Butyl 3-((2-(5-cyanopyrazin-2-ylamino)-5-(3-(ethoxycarbonyl)-1H-pyrrol-1-yl)pyridin-4-ylamino)methyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/384664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2,5-dimethoxy-tetrahydrofuran-3-carboxylate | HCID 19106911 | — |
| Reactant | Tert-butyl 3-((5-amino-2-(5-cyanopyrazin-2-ylamino)pyridin-4-ylamino)methyl)piperidine-1-carboxylate | HCID 66745373 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | tert-Butyl 3-((2-(5-cyanopyrazin-2-ylamino)-5-(3-(ethoxycarbonyl)-1H-pyrrol-1-yl)pyridin-4-ylamino)methyl)piperidine-1-carboxylate | HCID 71022175 | — |
Reaction Steps
tert-Butyl 3-((5-amino-2-(5-cyanopyrazin-2-ylamino)pyridin-4-ylamino)methyl)piperidine-1-carboxylate (163 mg, 0.384 mmol) (Synthesis 101-C) and ethyl 2,5-dimethoxy-tetrahydrofuran-3-carboxylate (196 mg, 0.96 mmol) were dissolved in acetic acid (4 mL) and the solution was stirred at 80° C. for 6.5 h. The reaction mixture was evaporated to dryness and the residue was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367658B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-ee4b1c7cbd714e9f90cde4e02245ec3e |
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| Source note | uspto-grants-2013_02 |
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