HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472907Generated: October 30, 2026
Trifluoroacetic acid → HCID 67215727, compound
https://huagongshe.com/reaction/472907
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 67215732 | HCID 67215732 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67215727 | HCID 67215727 | 97.8% |
Reaction Steps
1.3 ml of trifluoroacetic acid are added to 460 mg (1.01 mmol) of methyl 5-({6-[(tert-butoxycarbonyl)-(methyl)amino]imidazo[1,5-a]pyridin-3-yl}carbonyl)-2-nitrobenzoate in 5 ml of dichloromethane and the mixture is stirred at ambient temperature overnight. The reaction medium is concentrated under reduced pressure. The residue is taken up in water and basified with a saturated aqueous sodium bicarbonate solution and then extracted with dichloromethane. The organic phase is washed with a saturated aqueous sodium chloride solution, then dried over sodium sulfate and concentrated under reduced pressure. 350 mg of a red powder are obtained. Melting point: 183° C.; 1H NMR (d6-DMSO): 2.79 (3H, d), 3.90 (3H, s), 7.11 (1H, d), 7.77 (1H, s), 7.82 (1H, d), 8.31 (1H, d), 8.66 (1H, d), 8.75 (1H, s), 9.01 (1H, s)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633216B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-b062d6095e0a4916a5e14fc196bff003 |
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| Source note | uspto-grants-2014_01 |
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