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
Participants
| Role | Name | HCID | Charge |
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| Reactant | diethyl (1S,2S)-3,3-dimethylcyclopropane-1,2-dicarboxylate | HCID 2724581 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | N1-(4-bromobenzyl)-4-(quinolin-2-ylmethoxy)benzene-1,2-diamine | HCID 90414798 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | racemic trans-Ethyl 3-(1-(4-bromobenzyl)-5-(quinolin-2-ylmethoxy)-1H-benzo[d]imidazol-2-yl)-2,2-dimethylcyclopropanecarboxylate | HCID 117606232 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067917B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-6709175c508c4d55b762895798e5ca11 |
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| Source note | uspto-grants-2015_06 |
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