HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233676Generated: October 30, 2026
2-Aminothiazole → Thiourea, N-(3-phenylpropyl)-N'-2-thiazolyl-
https://huagongshe.com/reaction/233676
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminothiazole | HCID 2155 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Phenylpropyl isothiocynate | HCID 75815 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Thiourea, N-(3-phenylpropyl)-N'-2-thiazolyl- | HCID 3001100 | 16.5% |
Reaction Steps
A solution of 3-phenylpropyl isothiocyanate (500 mg, 2.82 mmol) and 2-aminothiazole (300 mg, 3.0 mmol) in N,N-dimethylformamide (10 mL) was heated to 100° C. After 20 h, the reaction was cooled to room temperature and poured into ethyl acetate. The organic phase was washed with 1N hydrochloric acid, water (3×), and brine. The organic layer was dried over sodium sulfate, filtered and concentrated. The solid obtained was purified by flash chromatography on silica gel (1% ethyl acetate in dichloromethane) and then recrystallized from ethyl acetate to provide 129 mg of the title product. A second crop was recrystallized from 1:1 ethyl acetate/hexanes to provide another 110 mg of the title product. Total yield of the title product: 239 mg (30%) as an off-white solid. A sample was recrystallized again from ethyl acetate:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05593993 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-9da61bc4048e4d7ea142ae175a9d7d4c |
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| Source note | uspto-grants-1997_01 |
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