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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrite | HCID 946 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hypophosphoric acid | HCID 24536 | — |
| Reactant | N6-propyl-4,5,6,7-tetrahydro-benzothiazole-2,6-diamine dihydrobromide | HCID 86651296 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | Propyl-(4,5,6,7-tetrahydro-benzothiazol-6-yl)-amine | HCID 18705889 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389555B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-a5d414f148fb479688f7c99dfe283d04 |
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| Source note | uspto-grants-2013_03 |
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