Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633971Generated: October 27, 2026

Acetic Acid → 4-[(4-tert-butylphenylamino)methyl]-N-(2H-tetrazol-5-yl)benzamide

https://huagongshe.com/reaction/1633971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-Tert-ButylanilineHCID 69861—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-formyl-N-(2H-tetrazol-5-yl)benzamideHCID 22501787—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTrimethyl orthoformateHCID 9005—
Product4-[(4-tert-butylphenylamino)methyl]-N-(2H-tetrazol-5-yl)benzamideHCID 22501763—

Reaction Conditions

Temperature25 °C

Reaction Steps

The above resin bound 4-formyl-N-(2H-tetrazol-5-yl)benzamide (500 mg) was treated with a 0.5 M solution of 4-tert-butylaniline (2.5 mmol, 412.5 mg) in a mixture of DMF and trimethylorthoformate (1:1, 5 mL) and glacial acetic acid (500 μL) for 1 hour at 25° C. followed by sodium cyanoborohydride (2.5 mmol, 160 mg) dissolved in a mixture of DMF and methanol (1:1, 2.5 mL). Shaking at 25° C. for 4 hours followed by filtration and washing with a mixture of methanol and DMF (1:1, 2×10 mL), DMF(3×10 mL) and dichloromethane (2×10 mL) afforded the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-ac20aac5f5fe472dbe9e5056dd2058ad
Source noteuspto-grants-2003_01