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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415293Generated: October 28, 2026

Ammonia → 2-(3-(Pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxamide

https://huagongshe.com/reaction/415293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethyl 2-(3-(pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxylateHCID 66621080—
SolventMethanolHCID 887—
Product2-(3-(Pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxamideHCID 6662118574%

Reaction Steps

Methyl 2-(3-(pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxylate (150 mg, 0.43 mmol) was added to ammonia in methanol (30 mL) and the mixture was stirred at room temperature for 3 days. Then the solid was filtered, washed with methanol, dried in vacuum. 100 mg of 2-(3-(pyridin-2-yl)phenyl)benzo[d]oxazole-7-carboxamide was obtained, yield: 74%. 1H-NMR (400 MHz, DMSO-d6) δ 7.44-7.47 (t, J=5.2 Hz, 1H), 7.50-7.54 (t, J=8.0 Hz, 1H), 7.76-7.88 (m, 3H), 7.96-8.01 (m, 3H), 8.12-8.14 (d, J=7.6 Hz, 1H); 8.35-8.39 (t, J=8.0 Hz, 2H); 8.76-8.77 (d, J=2.8 Hz, 1H); 9.01 (s, 1H); LC-MS (ESI) m/z: 316 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-9f6c0611c3e843c5aebf004e973f9de5
Source noteuspto-grants-2012_01