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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | (4-Amino-phenyl)-(1,3,3-trimethyl-6-aza-bicyclo[3.2.1]oct-6-yl)-methanone | HCID 577868 | — |
| Reactant | (2-trityl-2H-tetrazol-5-yl)-acetic acid | HCID 22405503 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-trityl-2H-tetrazol-5-yl-acetamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700583B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-03791ba44af04fc891d2e2255101534c |
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| Source note | uspto-grants-2010_04 |
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