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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907213Generated: October 30, 2026

Dimethylformamide → N-Trityl Losartan Carboxaldehyde

https://huagongshe.com/reaction/907213

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 (1a) 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, 10H), 7.53-7.58 (m, 2H), 7.84 (d, 1H), 9.73 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013005B2
Source datasetuspto-grants-2011_09
ORD IDord-678b3c58d1f143f6ab4adcf88f608f85
Source noteuspto-grants-2011_09