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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254124Generated: October 27, 2026

Hydrochloric Acid → HCID 178501566, compound

https://huagongshe.com/reaction/2254124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
ReactantMethyl bromoacetateHCID 60984—
Reactant5,6,7,8-tetrahydro-N-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-2-(trifluoromethyl)-4-quinazolinamineHCID 178506271—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178501566HCID 178501566—

Reaction Steps

To a 0° C. solution of 0.01 mmol of 5,6,7,8-tetrahydro-N-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-2-(trifluoromethyl)-4-quinazolinamine in 10 mL of anhydrous DMF was added 0.01 mmol of NaH. The resulting solution was stirred at 0° C. for 30 minutes at which time 0.01 mmol of triphenylmethylchloride was added. The reaction mixture was stirred at room temperature for 18 hours and 0.01 mmol of methyl bromoacetate was added. After 24 hours the reaction mixture was diluted with water and extracted with ethyl acetate (3×10 mL). The organic phase was extracted with brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield a residue which was treated with 2N HCl in dioxane. The solvents were evaporated and the resulting residue was purified on silica to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234936
Source datasetuspto-grants-1993_08
ORD IDord-0633c60b0e794137bb6099873d296fda
Source noteuspto-grants-1993_08