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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14294Generated: October 26, 2026

Methyl 3-[(dipropylamino)carbonyl]-5-(1,3-oxazol-2-yl)benzoate → 3-(Dipropylcarbamoyl)-5-(oxazol-2-yl)benzoic acid

https://huagongshe.com/reaction/14294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-[(dipropylamino)carbonyl]-5-(1,3-oxazol-2-yl)benzoateHCID 21939658—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventPotassium HydroxideHCID 14797—
Product3-(Dipropylcarbamoyl)-5-(oxazol-2-yl)benzoic acidHCID 2106289388.2%

Reaction Steps

A solution of methyl 3-[(dipropylamino)carbonyl]-5-(1,3-oxazol-2-yl)benzoate (315 mg, 0.95 mmol) in methanol (3 mL) and potassium hydroxide (3 mL of a 1.0 M solution in water, 3 mmol) was stirred at room temperature for 30 min. The solvent was removed under reduced pressure, the residue was dissolved in water, and extracted with ethyl acetate. The aqueous layer was acidified to pH 3 with 1 M hydrochloric acid, extracted with chloroform (3×100 mL), and the combined organic layers were concentrated under reduced pressure to afford 3-[(dipropylamino)carbonyl]-5-(1,3-oxazol-2-yl)benzoic acid (265 mg): 1H NMR (300 MHz, CD3OD) δ 8.71 (s, 1H), 8.08 (s, 2H), 8.05 (s, 1H), 7.34 (s, 1H), 3.52 (t, J=8 Hz, 2H), 3.26 (t, J=8 Hz, 2H), 1.75 (q, J=8 Hz, 2H), 1.59 (q, J=8 Hz, 2H), 1.02 (t, J=8 Hz, 3H), 0.74 (t, J=8 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-3a7444e147e44a8fa9befdd74e7df961
Source noteuspto-grants-2010_06