HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051896Generated: November 2, 2026
4-Bromobenzenesulfonamide → HCID 71736376, compound
https://huagongshe.com/reaction/1051896
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzenesulfonamide | HCID 69696 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 89813354 | HCID 89813354 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 71736376 | HCID 71736376 | 32.7% |
Reaction Steps
To a solution of 1-(4-(4-chlorophenyl)thiazol-2-yl)piperidin-2-one (Step 2 of compound 10, 0.5 g. 1.71 mmol) in dimethyl acetamide (5 ml) were added 4-bromobenzenesulfonamide (0.48 g, 2.05 mmol) and potassium acetate (0.42 g, 4.27 mmol) at 25° C. in a tube, the nitrogen gas was bubbled through reaction mixture for 15 minutes. To this was added palladium(II) acetate (0.02 g, 0.08 mmol) under nitrogen and the tube was sealed. The reaction mixture was heated at 150° C. for 15 hr under stirring. The progress of reaction was monitored by TLC. The reaction mixture was cooled to 25° C. and concentrated under reduced pressure. The residue was dissolved in ethyl acetate (30 ml), reaction mixture was washed with water (2×10 ml), dried over sodium sulphate and concentrated under reduced pressure to obtain a crude product; which was purified by preparative HPLC to obtain the title compound (0.25 g, 32.7%). MS: m/z 450 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388196B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-b29e80b86d6e4c0ba9a76d15a52af25a |
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| Source note | uspto-grants-2016_07 |
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