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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405855Generated: October 30, 2026

Propylphosphoric anhydride → HCID 178501909, compound

https://huagongshe.com/reaction/405855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylphosphoric anhydrideHCID 16167369—
ReactantMethyl 3-(3-(3-amino-4-methylphenyl)-1,2,4-oxadiazol-5-yl)azetidine-1-carboxylateHCID 86677444—
ReactantHCID 178524703HCID 178524703—
SolventEthyl AcetateHCID 8857—
ProductHCID 178501909HCID 178501909—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754071B2
Source datasetuspto-grants-2014_06
ORD IDord-319f3770da184255911f724e5c38ea81
Source noteuspto-grants-2014_06