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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719607Generated: October 29, 2026

Ammonium Bicarbonate → HCID 178513575, compound

https://huagongshe.com/reaction/719607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium BicarbonateHCID 14013—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 178513574HCID 178513574—
ReactantHCID 178524154HCID 178524154—
SolventDimethylformamideHCID 6228—
ProductHCID 178513575HCID 17851357576%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-[4-(2-Phenyl-[1,3]dioxolan-2-yl)-phenyl]-1H-benzoimidazole-5-carboxylic acid amide. To a solution of 2-{4-[2-(4-chloro-phenyl)-[1,3]dioxolan-2-yl]-phenyl}-1H-benzoimidazole-5-carboxylic acid (135 mg, 0.32 mmol) in anhydrous DMF was added carbonyldiimidazole (118 mg, 0.73 mmol). The reaction mixture was stirred under N2 for 30 min and then cooled to 0° C., and ammonium bicarbonate (140 mg, 1.4 mmol) was added. The resulting mixture was allowed to warm to RT and was stirred for 16 h. The mixture was added dropwise to saturated aqueous NH4Cl. The resulting precipitate was collected by filtration and washed with H2O (100 mL) then hexanes (100 mL). The product was dried under vacuum overnight to give the title compound (102 mg, 76%). TLC (silica, 1% methanol saturated with ammonia/9% methanol/CH2Cl2): Rf=0.33. HPLC (Method A): Rt=7.42. MS (ESI+): mass calculated for C23H18ClN3O3, 419.1; m/z found, 420.1 [M+H]+. 1H NMR (400 MHz, CD3OD): δ 8.09 (s, 1H), 8.00 (d, J=8.4 Hz, 2H), 7.75–7.72 (dd, J=8.5, 1.5 Hz, 1H), 7.59 (d, J=8.4 Hz, 2H), 7.56 (br d, J=8.7 Hz, 1H), 7.43 (d, J=8.5 Hz, 2H), 7.27 (d, J=8.6 Hz, 2H), 3.99 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132440B2
Source datasetuspto-grants-2006_11
ORD IDord-c3269ca197724632bb52e13e2141806b
Source noteuspto-grants-2006_11