HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930414Generated: November 1, 2026
Propylphosphonic anhydride → HCID 86732252, compound
https://huagongshe.com/reaction/930414
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | 5-Cyanopyridine-2-carboxylic acid | HCID 12400734 | — |
| Reactant | HCID 86732253 | HCID 86732253 | — |
| Product | HCID 86732252 | HCID 86732252 | 68.5% |
Reaction Steps
To a cooled (ice bath) solution of (4S,6S)-4-(5-amino-3-chloro-2-fluorophenyl)-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine (0.090 g, 0.276 mmol) and 5-cyano-2-pyridinecarboxylic acid (0.060 g, 0.405 mmol) in n,n-Dimethylformamide (1.5 mL) was added dropwise 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane 2,4,6-trioxide (0.352 mL, 0.553 mmol). After stirred for 1.5 h, reaction went to completion. The reaction mixture was quenched with saturated NaHCO3 and diluted with water. The resulted suspension was stirred for 30 min, and filtered. The filter caked was washed with water and purified by Shimadzu HPLC to afford the title compound (0.086 g, 0.189 mmol, 68.3% yield) as off-white solid. MS m/z=456.0 [M+H]+. Calculated for C19H14ClF4N5O2: 455.79
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296734B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-f4c317dacd5a43589f85ebbc2b8dc559 |
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| Source note | uspto-grants-2016_03 |
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