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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361357Generated: October 30, 2026

Dimethylformamide → N-Trityl Losartan Carboxaldehyde

https://huagongshe.com/reaction/1361357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazoleHCID 10053461—
ReactantHCID 178418251HCID 178418251—
SolventEthyl AcetateHCID 8857—
ProductN-Trityl Losartan CarboxaldehydeHCID 11657587—

Reaction Steps

To a DMF (150 mL) solution of 5-(4′-bromomethyl-biphenyl-2-yl)-1-trityl-1H-tetrazole (30 g, 53.8 mmol) was added 2-butyl-5-chloro-3H-imidazole-4-carbaldehyde (10 g, 53.8 mmol) and K2CO3 (7.4 g, 53.8 mmol). The mixture was stirred at room temperature overnight. EtOAc (500 mL) was added and the organic was washed three times with a NaHCO3 solution (200 mL) followed by saturated aqueous NaCl (200 mL). Solvent was removed and purification was achieved by silica gel chromatography (50:50 EtOAc:hexanes) using an isocratic gradient to provide intermediate (11a) a white solid (41 g). MS m/z: [M+H+] calcd for C41H35ClN6O, 663.26; found 663.4. 1H-NMR (d4-MeOH): 0.83 (m, 3H), 1.26 (m, 2H), 1.53 (m, 2H), 2.53 (m, 2H), 5.56 (s, 2H), 6.87-6.96 (m, 8H), 7.05 (m, 2H), 7.25-7.43 (m, 1OH), 7.53-7.58 (m, 2H), 7.84 (d, 1H), 9.73 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879896B2
Source datasetuspto-grants-2011_02
ORD IDord-2cf0a5e9b767483296e341531ee192cc
Source noteuspto-grants-2011_02