HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34652Generated: October 28, 2026
Hydrochloric Acid → (+/-)-4,5,5a,6,7,8-Hexahydro-6-propylthiazolo-[5,4-f]quinolin-2-amine
https://huagongshe.com/reaction/34652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21298204 | HCID 21298204 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (+/-)-4,5,5a,6,7,8-Hexahydro-6-propylthiazolo-[5,4-f]quinolin-2-amine | HCID 21298220 | — |
Reaction Steps
The free base of 4,5-dihydrothiazolo[5,4-f]quinolin-2-amine, 5.0 g (20 mmol), is refluxed in 250 ml ethanol with 6.8 g (40 mmol) of 1-iodopropane for 20 hours. The solvent is removed in-vacuo and the 2-amino-4,5-dihydrothiazolo[5,4-f]quinolinium iodide which remains is dissolved in 200 ml methanol and treated with 1.7 g (50 mmol) of sodium borohydride in small portions, at 0° C. After 1 hour, 50 ml of 10% hydrochloric acid is added dropwise and the volatile components are removed in-vacuo. The residue is made basic with ammonium hydroxide and extracted with ethyl acetate. The organic layer is dried over magnesium sulfate, evaporated and the residue is chromatographed to yield (±)-4,5,5a,6,7,8-hexahydro-6-propylthiazolo-[5,4-f]quinolin-2-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762843 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-ae31fdbebefb4ff897448c9bb33e46f9 |
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| Source note | uspto-grants-1988_08 |
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