HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280641Generated: October 28, 2026
Cyanoacetamide → 5-Amino-1-(4-[4-chlorobenzoyl]-3-chlorobenzyl)-1,2,3-triazole-4-carboxamide
https://huagongshe.com/reaction/280641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-(4-Chlorobenzoyl)-3-chlorobenzyl azide | HCID 13649661 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Amino-1-(4-[4-chlorobenzoyl]-3-chlorobenzyl)-1,2,3-triazole-4-carboxamide | HCID 10068949 | 32% |
Reaction Steps
A stirred suspension of 2-cyanoacetamide (378 mg, 4.50 mmol) in ethanol (15 ml) was treated with sodium methoxide (236 mg, 4.37 mmol), refluxed 10 minutes, cooled slightly, and treated with 4-(4-chlorobenzoyl)-3-chlorobenzyl azide (1.03 g, 3.36 mmol) dissolved in ethanol (4 ml). The mixture was refluxed 2 hours, cooled to ambient temperature, and filtered. The solids were washed with ethanol, and the combined filtrate and wash were evaporated to dryness under vacuum. The residue was dissolved in 19:1 (v/v) dichloromethane-methanol (40 ml) and chromatographed on a column of silica gel (60 g) eluted in 20 ml fractions with 97:3 (v/v) dichloromethane-methanol. Fractions 15-42 were combined and evaporated under vacuum to provide 402 mg (32%) of 5-amino-1-(4-[4-chlorobenzoyl]-3-chlorobenzyl)-1,2,3-triazole-4-carboxamide, m.p. 203°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04590201 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-f9cf472eee214c20add6e68628ce1608 |
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| Source note | uspto-grants-1986_05 |
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