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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415198Generated: October 29, 2026

Hydrochloric Acid → HCID 66621311, compound

https://huagongshe.com/reaction/415198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66621257HCID 66621257—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66621311HCID 6662131114.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 2-oxo-2-(2-(pyridin-4-yl)benzo[d]oxazol-4-yl)acetic acid (120 mg, 0.5 mmol) in DMF (15 mL) was added HOBt (148 mg, 1.1 mmol), NH4Cl (54 mg, 1.0 mmol), DIPEA (387 mg, 3.0 mmol) and EDCI (211 mg, 1.1 mmol). The mixture was stirred at 25° C. for 10 hr., water (10 mL) and 1N aqueous hydrochloric acid was added to the mixture until pH=3, then extracted with ethyl acetate (100 mL×4). The organic phase was washed with saturated sodium bicarbonate solution and brine, concentrated and dried in vacuum. The crude product was purified by preparative HPLC to obtain 2-(pyridin-4-yl)benzo[d]oxazole-4-carboxamide as a solid (17 mg, yield 14%). 1H-NMR (400 MHz, DMSO-d6) δ 7.60-7.64 (t, J=8 Hz, 1H), 8.01-8.03 (d, J=8 Hz, 1H), 8.06-8.08 (d, J=8 Hz, 2H), 8.23-8.24 (d, J=8 Hz, 2H), 8.41 (s, 1H), 8.87 (d, 2H); LC-MS (ESI) m/z 240 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-88cdeac949624c48845ba5532858f986
Source noteuspto-grants-2012_01