HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → Methyl 7-fluoro-6-(phenylamino)-1H-benzo[d]imidazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Methyl 4-amino-3-fluoro-5-nitro-2-(phenylamino)benzoate | HCID 44122658 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 7-fluoro-6-(phenylamino)-1H-benzo[d]imidazole-5-carboxylate | HCID 11818480 | 86.3% |
Reaction Steps
4-Amino-3-fluoro-5-nitro-2-phenylamino-benzoic acid methyl ester 26a (16.70 g, 54.71 mmol), formic acid (250 mL, 6.63 mol) and 20% Pd(OH)2/C (9.00 g, 16.91 mmol) in ethanol (250 mL) are stirred at 40° C. for two hours under N2 and then at 95° C. for 16 hours. The reaction mixture is cooled to room temperature and filtered through Celite rinsing with ethyl acetate. The filtrate is concentrated under reduced pressure to give a yellow solid. The solid is triturated with diethyl ether to give 13.47 g (86%) of the desired product as a tan solid. MS APCI (+) m/z 286 (M+1) detected; MS APCI (−) m/z 284 (M−1) detected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178693B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-cca60c5d483e4fc9874a2299b46eb43e |
| Source note | uspto-grants-2012_05 |