HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476294Generated: October 29, 2026
Sodium hydride → 3-(2'-t-Butoxycarbonylbiphenyl-4-ylmethyl)-7-methyl-2-propyl-3H-benzoimidazole-5-carboxylic acid methyl ester
https://huagongshe.com/reaction/476294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl 4'-(bromomethyl)biphenyl-2-carboxylate | HCID 9906257 | — |
| Reactant | 4-Methyl-2-propyl-1H-benzimidazole-6-carboxylic acid methyl ester | HCID 10130835 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(2'-t-Butoxycarbonylbiphenyl-4-ylmethyl)-7-methyl-2-propyl-3H-benzoimidazole-5-carboxylic acid methyl ester | HCID 68721756 | 74.7% |
Reaction Steps
A solution of 7-methyl-2-propyl-3H-benzoimidazole-5-carboxylic acid methyl ester (10.0 g, 43 mmol; prepared as described in Preparation 1) in DMF (300 mL) was cooled in an ice bath. Sodium hydride (4.5 g, 60 wt % in mineral oil) was slowly added over 5 minutes. 4′-Bromomethylbiphenyl-2-carboxylic acid t-butyl ester (15.7 g, 45.2 mmol; purchased from commercial source or prepared as described in Preparation 2) was then added. The mixture was gradually warmed to room temperature, then stirred at 75° C. overnight. The mixture was then cooled and concentrated in vacuo and the resultant residue was partitioned between saturated aqueous NaCl and EtOAc (1:1, 400 mL). The organic layer was collected, dried over MgSO4 and evaporated to dryness, yielding Intermediate (3a) as a pale yellow oil (16.0 g, 32.1 mmol). MS m/z: [M+H+] calcd for C31H34N2O4, 499.25. found 499.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637676B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-c5540af92e7747079268f6ce329ec19f |
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| Source note | uspto-grants-2014_01 |
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