HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463844Generated: November 3, 2026
Chloride → 1-(1-Naphthoyl)-3-[4-(5,6,7,8-tetrahydro-2-naphthyl)-2-thiazolyl]thiourea
https://huagongshe.com/reaction/1463844
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloride | HCID 312 | — |
| Reactant | 1-Naphthoic acid | HCID 6847 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | 2-Amino-4-(5,6,7,8-tetrahydro-2-naphthyl)thiazole | HCID 735091 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(1-Naphthoyl)-3-[4-(5,6,7,8-tetrahydro-2-naphthyl)-2-thiazolyl]thiourea | HCID 19088748 | 45.4% |
Reaction Steps
DMF (1 drop) was added to a solution of 1-naphthoic acid (900 mg) in THF (10 ml), followed by addition of oxayly chloride (0.49 ml) and stirring at room temperature for 2 hours. After replacing the solvent with acetone (10 ml), a solution of ammonium thiocyanate (436 mg) in acetone (5 ml) was added to the solution, followed by heating over a warm water bath for 1 minute and stirring at room temperature for 20 minutes. Then, a solution of 2-amino-4-(5,6,7,8-tetrahydro-2-naphthyl)thiazole (1,00 g) in acetone (10 ml) was added to the mixed solution, which was then stirred at room temperature for 16 hours. The reaction solution was poured into water, and the crystals which separated out were recovered by filtration and washed with diethyl ether. Recrystallization from dichloroethane-ethanol produced 1-(1-naphthoyl)-3-[4-(5,6,7,8-tetrahydro-2-naphthyl)-2-thiazolyl]thiourea (yield of 875 mg, 45.4%) in the form of colorless needles. m.p. 216°-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05302608 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-191cd670c6804b1ead7a1d542bb0b7f9 |
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| Source note | uspto-grants-1994_04 |
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