Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propanoyl bromide, 2-bromo- | HCID 79047 | — |
| Reactant | 5-Amino-1-(oxan-4-yl)-1H-pyrazole-4-carboxamide | HCID 42609131 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59418316 | HCID 59418316 | — |
Reaction Steps
A solution of C2 (5.0 g, 23.8 mmol) and triethylamine (3.65 mL, 26.2 mmol) in anhydrous DMF (50 mL) was cooled in an ice bath and treated drop-wise with 2-bromopropanoyl bromide (5.4 g, 25 mmol). The mixture was stirred at 0° C. for 30 mins, warmed to room temperature and stirred at ambient temperature for an additional 2 h. The reaction was partitioned between EtOAc (200 mL) and aqueous 2N hydrochloric acid (500 mL); the organic phase was washed with saturated aqueous sodium bicarbonate solution (400 mL), saturated aqueous sodium chloride solution (200 mL) and dried over sodium sulfate. Filtration and concentration of the filtrate provided crude C24 as an orange residue, which was used in the next step without purification,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618117B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-2e212b0589eb43cc8fcfff14e4f62105 |
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| Source note | uspto-grants-2013_12 |
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