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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633975Generated: October 26, 2026

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

https://huagongshe.com/reaction/1633975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-tert-ButylcyclohexylamineHCID 79396—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-formyl-N-(2H-tetrazol-5-yl)benzamideHCID 22501787—
SolventMethanolHCID 887—
SolventTrimethyl orthoformateHCID 9005—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-[(4-tert-butylcyclohexylamino)methyl]-N-(2H-tetrazol-5-yl)benzamideHCID 22502404—

Reaction Conditions

Temperature25 °C

Reaction Steps

The above resin bound 4-formyl-N-(2H-tetrazol-5-yl)benzamide (50 mg) was treated with a 0.5 M solution of 4-tert-butylcyclohexylamine (0.25 mmol, 38.75 mg) in a mixture of NMP and trimethylorthoformate (1:1, 0.5 mL) and glacial acetic acid (50 μL) for 1 hour at 25° C. followed by sodium cyanoborohydride (250 μmol, 16 mg) dissolved in a mixture of NMP and methanol (1:1, 0.25 mL). Shaking at 25° C. for 4 hours followed by filtration and washing with a mixture of NMP and methanol (1:1, 2×1 mL), NMP (3×1 mL) and a mixture of 1,2-dichloropropane (DCP) and diisopropylethylamine (7:1, 2×1 mL) afforded the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-58ba27b381b54005aa08ae67793e89f5
Source noteuspto-grants-2003_01