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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942335Generated: October 26, 2026

Nitrite → Propyl-(4,5,6,7-tetrahydro-benzothiazol-6-yl)-amine

https://huagongshe.com/reaction/1942335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitriteHCID 946—
ReactantSodium HydroxideHCID 14798—
ReactantHypophosphoric acidHCID 24536—
ReactantN6-propyl-4,5,6,7-tetrahydro-benzothiazole-2,6-diamine dihydrobromideHCID 86651296—
SolventHydrochloric AcidHCID 313—
ProductPropyl-(4,5,6,7-tetrahydro-benzothiazol-6-yl)-amineHCID 18705889—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 14.5 g (38.9 mmol) N6-propyl-4,5,6,7-tetrahydro-benzothiazole-2,6-diamine dihydrobromide in 220 mL concentrated aqueous hydrochloric acid at −30° C. is drop wise added 66.3 mL of an aqueous 1N solution nitrite over the course of 30 minutes. After further stirring for 1 hour at the same temperature 5.44 ml (52.5 mmol) of a 50% aqueous solution hypophosphoric acid is added. The reaction mixture is stored at 4° C. overnight. After having cooled down the solution again to −30° C. the mixture is slowly basified with 40% aqueous sodium hydroxide solution while temperature is kept at −30° C. The resulting mixture is warmed up to room temperature and extracted with Chloroform/Ethanol 5:1 (3×250 mL) The solution is dried over anhydrous sodium sulfate and concentrated in vacuum. The brown oil obtained is chromatographed over silica gel, eluting with dichloromethane/methanol 97:3 under ammonia atmosphere.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389555B2
Source datasetuspto-grants-2013_03
ORD IDord-a5d414f148fb479688f7c99dfe283d04
Source noteuspto-grants-2013_03