HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948422Generated: October 30, 2026
Triethylamine → N-{5-[2-Bromo-5-(1-methyl-piperidin-4-ylsulfamoyl)-thiophen-3-yl]-4-methyl-thiazol-2-yl}-acetamide
https://huagongshe.com/reaction/1948422
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| Reactant | 4-[2-(Acetylamino)-4-methyl-1,3-thiazol-5-yl]-5-bromothiophene-2-sulfonylchloride | HCID 86623146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{5-[2-Bromo-5-(1-methyl-piperidin-4-ylsulfamoyl)-thiophen-3-yl]-4-methyl-thiazol-2-yl}-acetamide | HCID 86652443 | 74% |
Reaction Steps
4-[2-(acetylamino)-4-methyl-1,3-thiazol-5-yl]-5-bromothiophene-2-sulfonyl chloride, prepared as in Step III of Example 23 (200 mg; 0.48 mmol; 1 eq), is dissolved in anhydrous DCM (10 ml). The reaction mixture is cooled down to 0° C. and put under nitrogen. Triethylamine (0.27 ml; 1.92 mmol; 4 eq) and 1-methyl-piperidin-4-ylamine (0.11 ml; 0.96 mmol; 2 eq) are added successively and the reaction mixture is stirred at 0° C. for 40 minutes. It is then washed with water, NaHCO3 and dried over MgSO4, affording the title compound (185 mg; 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399497B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-8afe9d92e21149169c90335ec5eb3d02 |
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| Source note | uspto-grants-2013_03 |
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