HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenecarbonyl chloride → N-(4H-indeno[1,2-d][1,3]thiazol-2-yl)thiophene-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenecarbonyl chloride | HCID 78928 | — |
| Reactant | HCID 49796119 | HCID 49796119 | — |
| Product | N-(4H-indeno[1,2-d][1,3]thiazol-2-yl)thiophene-2-carboxamide | HCID 2727911 | 17.8% |
Reaction Steps
Acylation 8H-Indeno[1,2-d]thiazol-2-ylamine hydroiodide 1a (Prepared in Example 1, Step 1, 100 mg; 0.32 mmol) with 2-thiophenecarbonyl chloride (0.106 mL; 0.96 mmol) in a manner similar to that described in Example 1, Step 3 provided 17 mg of Thiophene-2-carboxylic acid (8H-indeno[1,2-d]thiazol-2-yl)-amide 6. EI-HRMS m/e calcd for C15H10N2OS2 (M+) 298.0235, found 298.0233.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07407977B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-209b4b693932480ea04802e0c25fa493 |
| Source note | uspto-grants-2008_08 |