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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472143Generated: November 2, 2026

Ammonium Chloride → N-(benzo[d]thiazole-2-yl)-2-(2H-tetrazole-5-yl)acetamide

https://huagongshe.com/reaction/1472143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantN-(1,3-benzothiazol-2-yl)-2-cyanoacetamideHCID 4530340—
SolventDimethylformamideHCID 6228—
ProductN-(benzo[d]thiazole-2-yl)-2-(2H-tetrazole-5-yl)acetamideHCID 8666069420%

Reaction Conditions

Temperature120 °C

Reaction Steps

N-(benzo[d]thiazole-2-yl)-2-cyanoacetamide (0.1 g), NH4Cl (5.0 eq, 0.1 g), and NaN3 (5.2 eq, 0.13 g) were dissolved on 2.1 mL of DMF (dimethylformamide), and heated at 120° C. for 6 hours. DMF was removed under reduced pressure distillation, and 10 ml of water and 5% NaOH solution were added thereto. The aqueous layer was washed with 15 ml of Et2O, and treated with activated carbon. To the obtained reaction mixture, 10% aqueous hydrochloric acid, making the solution with pH 2. The obtained reaction mixture was extracted with methylene chloride, to produce N-(benzo[d]thiazole-2-yl)-2-(2H-tetrazole-5-yl)acetamide (20%, 21 mg) in light yellow solid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012481B2
Source datasetuspto-grants-2015_04
ORD IDord-5ebc77ace50a49899e646e4287a3be39
Source noteuspto-grants-2015_04