HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288295Generated: November 2, 2026
Sulfuric Acid → 1-Benzyl-5-isovaleramido-4-isovalerylcarbamoyl-1,2,3-triazole
https://huagongshe.com/reaction/1288295
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isovaleryl chloride | HCID 66054 | — |
| Reactant | 5-Amino-1-benzyl-1H-1,2,3-triazole-4-carboxamide | HCID 225435 | — |
| Product | 1-Benzyl-5-isovaleramido-4-isovalerylcarbamoyl-1,2,3-triazole | HCID 21504354 | — |
Reaction Steps
Concentrated sulphuric acid (7.5 ml.) was added dropwise, under anhydrous conditions, to an ice-cooled, stirred suspension of 5-amino-1-benzyl-4-carbamoyl-1,2,3-triazole (10.85 g.; prepared as described by J. R. E. Hoover and A. R. Day, J.Amer.Chem.Soc., 1956, 78, 5832) in isovaleryl chloride (50 ml.), and the mixture was then stirred at room temperature overnight. The resulting solution was poured into ice-water, and the precipitated solid filtered off, stirred well with water, again filtered off, and dried, to give 1-benzyl-5-isovaleramido-4-isovalerylcarbamoyl-1,2,3-triazole (16.4 g.), m.p. 125°-128° C. An aliquot was recrystallised from di-isopropyl ether to give pure 1benzyl-5-isovaleramido-4-isovalerylcarbamoyl-1,2,3-triazole, m.p. 130°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03987160 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-0d110f42e5c64db6a7c4174244879e04 |
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| Source note | uspto-grants-1976_10 |
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