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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415195Generated: October 30, 2026

Hydrochloric Acid → HCID 46847289, compound

https://huagongshe.com/reaction/415195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66621013HCID 66621013—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 46847289HCID 468472894.15%

Reaction Steps

2-(4-bromophenyl)benzo[d]oxazole-4-carboxylic acid (0.075 g, 0.24 mmol) in dimethyl formamide (10 mL) was added HOBT (0.0425 g, 0.28 mmol), EDCI (0.0575 g, 0.3 mmol), DIPEA (0.097 g, 0.75 mmol) and ammonium chloride (0.0133 g, 0.25 mmol). The reaction mixture was stirred at room temperature for 20 hr, cooled and poured into water (10 mL). The solution was acidified to pH=3 with 1N aqueous hydrochloric acid. Then the solution was extracted with dichloromethane (70 mL×3). The organic layer was washed with brine, dried over anhydrous sodium sulfate, condensed in vacuum and separated by silica gel chromatography (ethyl acetate:methanol=1:0 to 10:1) to afford 2-(4-bromophenyl)benzo[d]oxazole-4-carboxamide as a solid (0.003 g, yield 4.15%). LC-MS (ESI) m/z 319 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-999c29bbf6b94e738ebc2613f2538bd9
Source noteuspto-grants-2012_01