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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643263Generated: October 28, 2026

1,1'-Carbonyldiimidazole → 2-trityl-2H-tetrazol-5-yl-acetamide

https://huagongshe.com/reaction/643263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(4-Amino-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanoneHCID 577868—
Reactant(2-trityl-2H-tetrazol-5-yl)-acetic acidHCID 22405503—
SolventTetrahydrofuranHCID 8028—
Product2-trityl-2H-tetrazol-5-yl-acetamideHCID 131728059—

Reaction Steps

To a solution of (2-trityl-2H-tetrazol-5-yl)-acetic acid (0.82 g, 2.20 mmol) in dry THF (50 ml) was added CDI (0.4 g, 2.39 mmol) and the resulting mixture was stirred for 10 min. To this mixture was added (4-amino-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone (0.5 g, 1.84 mmol) and the stirring was continued for 18 hrs. at room temperature. The mixture was evaporated and the residue purified by column chromatography (silica gel) using EtOAc-Heptane (4:1) as eluent. Pure fractions were collected and evaporated to dryness affording 150 mg (13%) of N-[4-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]octane-6-carbonyl)-phenyl]-2-(2-trityl-2H-tetrazol-5-yl-acetamide which was dissolved in THF (25 ml) followed by addition of 20% aqueous HCl (20 ml). The mixture was stirred for 2 hrs. at room temperature at which time the volatiles were removed in vacuo. The aqueous residue was extracted with EtOAc (2×50 ml), dried (Na2SO4), filtered and evaporated in vacuo affording 30 mg (4%) of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700583B2
Source datasetuspto-grants-2010_04
ORD IDord-03791ba44af04fc891d2e2255101534c
Source noteuspto-grants-2010_04