HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Sulfamoylbenzene-1-carbothioamide → 3-[4-(4-Ethylpyridin-3-yl)-1,3-thiazol-2-yl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Sulfamoylbenzene-1-carbothioamide | HCID 5151236 | — |
| Reactant | 2-Bromo-1-(4-ethylpyridin-3-yl)ethanone | HCID 22049794 | — |
| Product | 3-[4-(4-Ethylpyridin-3-yl)-1,3-thiazol-2-yl]benzenesulfonamide | HCID 22049774 | 38.1% |
Reaction Steps
By the reaction in the same manner as in Example 25-iii) using 2-bromo-1-(4-ethylpyridin-3-yl)ethanone hydrobromate (161 mg) and 3-(aminosulfonyl)benzenecarbothioamide (110 mg), the title compound (67 mg) was obtained as colorless powder crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067537B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-762e0dbfe02f4eb6b64ad1d87825bcae |
| Source note | uspto-grants-2006_06 |