HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 86662194, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66742610 | HCID 66742610 | — |
| Reactant | HCID 86662195 | HCID 86662195 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86662194 | HCID 86662194 | — |
Reaction Steps
The title compound was prepared according to the general procedure (Method A) by coupling Intermediate 1 (30 mg, 0.167 mmol) with 2-bromo-N-{4-[3,5-difluoro-4-(3,3,3-trifluoropropoxy)phenyl]-1,3-thiazol-2-yl}acetamide (89 mg, 0.200 mmol) in the presence of NaH (10 mg, 0.416 mmol) in dry DMF (5.0 mL) to give 18 mg of the product as a white solid; 1H NMR (δ ppm, DMSO-d6, 300 MHz): 2.73-2.84 (m, 2H), 3.17 (s, 3H), 3.39 (s, 3H), 4.32-4.38 (m, 2H), 5.32 (s, 2H), 6.23 (s, 1H), 7.35 (s, 1H), 7.66 (s, 1H), 7.69 (s, 1H), 7.80 (s, 1H), 12.70 (br s, 1H); APCI-MS (m/z): 542.20 [M−H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09000159B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-c4b189c45e2b444e80997ed80333c132 |
| Source note | uspto-grants-2015_04 |