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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529014Generated: October 29, 2026

Benzyl Bromide → 3-Benzyl 1-methyl 4-(1-benzyl-4-(dibutylcarbamoyl)-1H-imidazol-2-yl)isophthalate

https://huagongshe.com/reaction/529014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 178449065HCID 178449065—
Product3-Benzyl 1-methyl 4-(1-benzyl-4-(dibutylcarbamoyl)-1H-imidazol-2-yl)isophthalateHCID 8671893477.4%

Reaction Steps

Following a procedure analogous to that for the synthesis of Intermediate 271F, 3-benzyl 1-methyl 4-(4-(dibutylcarbamoyl)-1H-imidazol-2-yl)isophthalate (200 mg, 0.40 mmol) and benzylbromide (83 mg, 0.48 mmol) were converted to the title compound (180 mg, 76%). 1H NMR (CDCl3) 8.68 (d, J=1.6 Hz, 1H), 8.15 (dd, J=8.0, 2.0 Hz, 1H), 7.43 (s, 1H), 7.39-7.34 (m, 4H), 7.28-7.26 (m, 2H), 7.21-7.17 (m, 3H), 6.90-6.88 (m, 2H), 5.15 (s, 2H), 4.64 (s, 2H), 3.96 (s, 3H), 3.90 (br s, 2H), 3.43 (br s, 2H), 1.70-1.59 (m, 4H), 1.37-1.23 (m, 4H), 0.93-0.82 (m, 6H); MS(ESI+) m/z 582.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346795B2
Source datasetuspto-grants-2016_05
ORD IDord-75b72ddaeebf47b898db43ec111509af
Source noteuspto-grants-2016_05