HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861167Generated: October 31, 2026
Trifluoroacetic acid → HCID 178489105, compound
https://huagongshe.com/reaction/861167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178489104 | HCID 178489104 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178489105 | HCID 178489105 | 33% |
Reaction Steps
To a solution of N,N″-di-tert-butoxycarbonyl-N′-(4-{[3-[2-(cyclopentylamino)-pyrimidin-4-yl]-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-7-yl]amino}butyl)-guanidine (42 mg, 0.06 mmol) in dichloromethane (8 mL) was added trifluoroacetic acid (2 mL). The resultant solution was stirred for 8 hours and then concentrated in vacuo. The residue was dissolved in dichloromethane and saturated aqueous sodium bicarbonate was added. The organic layer was washed with brine. The aqueous layer was extracted with dichloromethane and the combined organics were dried over sodium sulfate. Filtration and concentration provided N-(4-{[3-[2-(cyclopentylamino)pyrimidin-4-yl]-2-(4-methoxyphenyl)pyrazolo[1,5-a]pyridin-7-yl]amino}butyl)guanidine (10 mg, 33%) as a yellow solid. MS m/z 514 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153855B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-c15ec04545944763804bc7b3aedf8de5 |
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| Source note | uspto-grants-2006_12 |
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