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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415239Generated: October 28, 2026

Hydrochloric Acid → HCID 86633089, compound

https://huagongshe.com/reaction/415239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86633090HCID 86633090—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86633089HCID 866330893%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of methyl 2-(4-methoxyphenylbenzo[d]oxazole-7-carboxylate 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. To the resulting mixture, water (10 mL) and aqueous hydrochloric acid (1 N) were added to 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 pre-HPLC to obtain 2-(4-methoxyphenylbenzo[d]oxazole-7-carboxamide as a white solid (8 mg, yield 3% for 2 steps). 1H-NMR (400 MHz, CDCl3-d) δ 3.93 (s, 3H), 6.16 (s, 1H), 7.06-7.08 (d, J=8 Hz, 3H), 7.47 (s, 1H), 7.90-8.18 (m, 4H); LC-MS (ESI) m/z 269 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-c828d6b7b0d049cf82e5ab5c52215922
Source noteuspto-grants-2012_01