HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045478Generated: October 31, 2026
Propylphosphoric anhydride → HCID 178501909, compound
https://huagongshe.com/reaction/1045478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylphosphoric anhydride | HCID 16167369 | — |
| Reactant | Methyl 3-(3-(3-amino-4-methylphenyl)-1,2,4-oxadiazol-5-yl)azetidine-1-carboxylate | HCID 86677444 | — |
| Reactant | HCID 178524703 | HCID 178524703 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178501909 | HCID 178501909 | — |
Reaction Steps
To a stirring solution of 7-(1H-pyrazol-3-yl)imidazo[1,2-a]pyridine-3-carboxylic acid (63) (31.7 mg, 0.14 mmol), and methyl (3-(3-amino-4-methylphenyl)-1,2,4-oxadiazol-5-yl)methylcarbamate (31) (52 mg, 0.18 mmol) in ethyl acetate (0.1 mL) was added propylphosphonic anhydride (50 wt % in ethyl acetate 0.41 mL). The reaction was heated at 80° C. for 12 hours. The resulting mixture was diluted in ethyl acetate and washed with 1N Na2CO3. After aqueous workup, the residue was purified by reverse phase HPLC to afford methyl 3-(3-(3-(7-(1H-pyrazol-3-yl)imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)azetidine-1-carboxylate (F68). MS (m/z) 499.1 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569283B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-ec1d46249ac54f248f0b7a276a1ef502 |
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| Source note | uspto-grants-2013_10 |
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