HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076128Generated: October 25, 2026
Potassium Carbonate → [3-Methoxy-4-(2-methyl-thiazol-5-yl)-phenyl]-thiourea
https://huagongshe.com/reaction/2076128
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 3-Methoxy-4-(2-methyl-thiazol-5-yl)-phenylamine | HCID 67095903 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-Methoxy-4-(2-methyl-thiazol-5-yl)-phenyl]-thiourea | HCID 86632612 | 89.9% |
Reaction Steps
To a solution of 3-methoxy-4-(2-methyl-thiazol-5-yl)-phenylamine (100 mg, 0.45 mmol) in tetrahydrofurane (4 mL) was added drop wise under stirring and under an atmosphere benzoyl isothiocyanate (67.7 ul, 0.48 mmol). The reaction was stirred at room temperature for 3 hours and the solvent was removed under reduced pressure. The residue was dissolved in methanol (6 mL) and a solution of potassium carbonate (188 mg, 1.36 mmol) in water (3 mL) was added. The resulting suspension was stirred at room temperature over night. The precipitate was filtered off, washed with water and diethyl ether to yield the title compound as a pale yellow solid (113 mg, 89%). MS ISP (m/e): 280.1 (100%) [(M+H)+]. 1H NMR (DMSO-D6, 300 MHz): δ (ppm)=9.82 (s, 1H, NH), 8.02 (s, 1H), 7.62 (d, 1H), 7.40 (s, 1H), 7.01 (s, 1H), 3.87 (s, 3H), 2.64 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07923450B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-ff05bce50acb4c159253c20a01d47aa2 |
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| Source note | uspto-grants-2011_04 |
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