HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067028Generated: October 31, 2026
Formic Acid → 8-(4-Bromo-2-chloro-phenylamino)-imidazo[1,5-a]pyridine-7-carboxylic acid (2-hydroxy-ethoxy)-amide
https://huagongshe.com/reaction/2067028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 8-(4-Bromo-2-chloro-phenylamino)-imidazo[1,5-a]pyridine-7-carboxylic acid (2-vinyloxy-ethoxy)-amide | HCID 59565223 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-(4-Bromo-2-chloro-phenylamino)-imidazo[1,5-a]pyridine-7-carboxylic acid (2-hydroxy-ethoxy)-amide | HCID 44137364 | 23.5% |
Reaction Steps
8-(4-Bromo-2-chloro-phenylamino)-imidazo[1,5-a]pyridine-7-carboxylic acid (2-vinyloxy-ethoxy)-amide (196 mg, 0.43 mmol) was dissolved in methanol and loaded onto an Isolute® SCX-2 cartridge (10 g). The cartridge was then washed with methanol and the desired product was subsequently eluted using 2M NH3 in MeOH. Appropriate fractions were combined and concentrated to give a residue that was subjected to flash chromatography (Si-PPC, gradient 0% to 10%, methanol in dichloromethane). The appropriate fractions were combined and concentrated to give a residue that was subjected to HPLC (Preparative C18 column, 0.1% formic acid, acetonitrile in water, gradient 5% to 98%, ramp time 20 minutes) to afford the title compound as a pale yellow solid (43 mg, 23%). LCMS (method A): RT=6.71 min, [M+H]+=425/427. 1H NMR (DMSO-d6): 11.68 (1H, s), 10.46 (1H, s), 8.35 (1H, d, J=0.79 Hz), 7.95 (1H, d, J=7.36 Hz), 7.78 (1H, d, J=2.27 Hz), 7.42 (1H, dd, J=8.62, 2.29 Hz), 7.01 (1H, d, J=8.63 Hz), 6.79 (1H, d, J=7.35 Hz), 6.56 (1H, s), 4.69 (1H, s), 3.87 (2H, t, J=4.89 Hz), 3.57 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293763B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-8712c3f2a38f410584813cb7656d39e4 |
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| Source note | uspto-grants-2012_10 |
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