Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formamide | HCID 713 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 59447959 | HCID 59447959 | — |
| Product | HCID 178518049 | HCID 178518049 | — |
Reaction Steps
2-Amino-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid ethyl ester (600 mg, 3 mmol) and ammonium formate (185 mg, 3 mmol) were suspended in 10 mL formamide and heated at 175° C. for 5 hours. Water was added to the cooled reaction mixture and the resulting precipitate collected and dried in vacuo. Unprecipitated product was recovered from the filtrate by using a MP-TsOH SPE cartridge and eluting with 7 N ammonia to give a combined mass of 330 mg of the title compound. LCMS (1): Rt 0.67 min; m/z 188 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618121B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-79ddaec2c6ea49238e826a82ab110423 |
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| Source note | uspto-grants-2013_12 |
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