HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(5-Iodo-4-methyl-2-thiazolyl)acetamide → HCID 86620380, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(5-Iodo-4-methyl-2-thiazolyl)acetamide | HCID 57417074 | — |
| Reactant | 5-Bromo-N-(2-hydroxyethyl)-3-pyridinesulfonamide | HCID 61795523 | — |
| Product | HCID 86620380 | HCID 86620380 | 23% |
Reaction Steps
Using an analogous method to that described in Example 7, N-(5-iodo-4-methyl-1,3-thiazol-2-yl)acetamide was reacted with 5-bromo-N-(2-hydroxyethyl)pyridine-3-sulfonamide to give the title compound (Method A HPLC: retention time 4.0 minutes; 10 mg, 23%); 1H NMR Spectrum: (DMSOd6) 12.22 (1H, br s); 8.92 (1H, d); 8.86 (1H, d); 8.16 (1H, t); 7.96 (1H, br s); 4.73 (1H, t); 3.39 (2H, br q); 2.89 (2H, br t); 2.40 (3H, s); 2.17 (3H, s); Mass Spectrum: M+H+ 357.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868188B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-83ad2c1c82fb4ccd81e3b61fc120a503 |
| Source note | uspto-grants-2011_01 |