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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Tert-Butylaniline | HCID 69861 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-formyl-N-(2H-tetrazol-5-yl)benzamide | HCID 22501787 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Trimethyl orthoformate | HCID 9005 | — |
| Product | 4-[(4-tert-butylphenylamino)methyl]-N-(2H-tetrazol-5-yl)benzamide | HCID 22501763 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06503949B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-ac20aac5f5fe472dbe9e5056dd2058ad |
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| Source note | uspto-grants-2003_01 |
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