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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55331Generated: October 28, 2026

1-[2-[4-(2-Methoxycarbonyl-2-methylpropyl)phenyl]ethyl]-1,5-diazacyclooctane → 1-[1-(4-chlorophenylmethyl)-1H-benzimidazol-2-yl]-5-[2-[4-(2-methoxycarbonyl-2-methylpropyl)phenyl]ethyl]-1,5-diazacyclooctane

https://huagongshe.com/reaction/55331

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[2-[4-(2-Methoxycarbonyl-2-methylpropyl)phenyl]ethyl]-1,5-diazacyclooctaneHCID 19957513—
Reactant2-bromo-1-(4-chlorophenylmethyl)-1H-benzimidazoleHCID 19957517—
Solvent1-ButanolHCID 263—
Product1-[1-(4-chlorophenylmethyl)-1H-benzimidazol-2-yl]-5-[2-[4-(2-methoxycarbonyl-2-methylpropyl)phenyl]ethyl]-1,5-diazacyclooctaneHCID 1995751458%

Reaction Steps

To a solution of 2-bromo-1-(4-chlorophenylmethyl)-1H-benzimidazole (0.029 g) in n-butanol (0.5 ml) was added 1-[2-[4-(2-methoxycarbonyl-2-methylpropyl)phenyl]ethyl]-1,5-diazacyclooctane (0.102 g), and the mixture was refluxed for 3 hours. The reaction mixture was quenched with a saturated aqueous NaHCO3 solution (30 ml), and the mixture was extracted with methylene chloride (20 ml). The extract was washed with water, and dried over anhydrous MgSO4. The solvent was removed under reduced pressure, and the residue was purified by medium pressure liquid column chromatography on a silica gel column using a mixture of methylene chloride, diethyl ether and methanol (1:1:0.2) as eluent to give 1-[1-(4-chlorophenylmethyl)-1H-benzimidazol-2-yl]-5-[2-[4-(2-methoxycarbonyl-2-methylpropyl)phenyl]ethyl]-1,5-diazacyclooctane (0.030 g) as a colorless oily liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624948
Source datasetuspto-grants-1997_04
ORD IDord-e73b6b9de0744504bd3c6e59ec7f1560
Source noteuspto-grants-1997_04