HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088491Generated: November 2, 2026
Potassium Carbonate → HCID 68430980, compound
https://huagongshe.com/reaction/2088491
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 5-Bromo-4-methylthiophene-2-carbaldehyde | HCID 16414192 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68430980 | HCID 68430980 | 83% |
Reaction Steps
The mixed solution of 5-bromo-4-methyl-thiophene-2-carbaldehyde (k) (0.93 mmol) in methanol (4 mL) was added tosylmethyl isocyanide (1.02 mmol) and K2CO3 (1.88 mmol). The reaction was stirred at room temperature for 5 min before heated to 80° C. in the sealed tube. After 30 min, the solution was cooled to room temperature and concentrated. Column chromatography afforded 5-bromo-4-methyl-5-(oxazol-5-yl)-thiophene (l) (190 mg, 80%). Compound (n) was prepared using a Suzuki Coupling reaction analogous to step B of the preparation of Example 1. 1-(2,6-difluoro-phenyl)-3-[4-(5-oxazol-5-yl-3-methyl-thiophen-2-yl)-phenyl]-urea was prepared by reacting (n) with 2,6-difluorophenyl isocyanate by an analogous procedure as that described for Example 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08435996B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-931449952935413cab8c5c8efab69322 |
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| Source note | uspto-grants-2013_05 |
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