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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantIsovaleryl chlorideHCID 66054—
Reactant5-Amino-1-benzyl-1H-1,2,3-triazole-4-carboxamideHCID 225435—
Product1-Benzyl-5-isovaleramido-4-isovalerylcarbamoyl-1,2,3-triazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987160
Source datasetuspto-grants-1976_10
ORD IDord-0d110f42e5c64db6a7c4174244879e04
Source noteuspto-grants-1976_10