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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178418Generated: October 31, 2026

diethyl (1S,2S)-3,3-dimethylcyclopropane-1,2-dicarboxylate → racemic trans-Ethyl 3-(1-(4-bromobenzyl)-5-(quinolin-2-ylmethoxy)-1H-benzo[d]imidazol-2-yl)-2,2-dimethylcyclopropanecarboxylate

https://huagongshe.com/reaction/2178418

Reaction equation

Participants

RoleNameHCIDCharge
Reactantdiethyl (1S,2S)-3,3-dimethylcyclopropane-1,2-dicarboxylateHCID 2724581—
ReactantTrimethylaluminumHCID 16682925—
ReactantN1-(4-bromobenzyl)-4-(quinolin-2-ylmethoxy)benzene-1,2-diamineHCID 90414798—
SolventDichloromethaneHCID 6344—
Productracemic trans-Ethyl 3-(1-(4-bromobenzyl)-5-(quinolin-2-ylmethoxy)-1H-benzo[d]imidazol-2-yl)-2,2-dimethylcyclopropanecarboxylateHCID 117606232—

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of trimethyl aluminum (0.2 mL, 2 M in toluene) was added to 25 mL round-bottomed flask containing N1-(4-bromobenzyl)-4-(quinolin-2-ylmethoxy)benzene-1,2-diamine (100 mg, 0.23 mmol), trans-diethyl 3,3-dimethylcyclopropane-1,2-dicarboxylate (49 mg, 0.23 mmol), and DCM (4 mL). After 12 h, the solution was partitioned between sat. NaHCO3 (30 mL) and EtOAc (30 mL). The organic layer was separated and the aqueous layer was extracted with EtOAc (2×30 mL). The combine organic layers were dried with sodium sulfate, filtered, and concentrated to dryness. To the residue was added ethanol (2 mL) and concentrated HCl (0.1 mL, 12 N). The solution heated to 90° C. After 5 h, the mixture was cooled, concentrated to dryness, and purified by reverse phase HPLC to afford the title compound. MS (ESI): mass calcd. for C32H30BrN3O3, 583.15; m/z found, 584.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067917B2
Source datasetuspto-grants-2015_06
ORD IDord-6709175c508c4d55b762895798e5ca11
Source noteuspto-grants-2015_06