HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 46947434, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66742610 | HCID 66742610 | — |
| Reactant | HCID 86662188 | HCID 86662188 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 46947434 | HCID 46947434 | — |
Reaction Steps
The title compound was prepared according to the general procedure (Method A) by coupling Intermediate 1 (50 mg, 0.279 mmol) with 2-bromo-N-{4-[4-(2-methylpropoxy)-3,5-difluorophenyl]-1,3-thiazol-2-yl}acetamide (135 mg, 0.334 mmol) in the presence of NaH (10 mg, 0.416 mmol) in dry DMF (5.0 mL) to give 45 mg of the product as an off-white solid; 1H NMR (δ ppm, 300 MHz, DMSO-d6) 0.98 (d, J=6.9 Hz, 6H), 1.96-2.04 (m, 1H), 3.17 (s, 3H), 3.33 (s, 3H), 3.91 (d, J=6.3 Hz, 2H), 5.32 (s, 2H), 6.22 (s, 1H), 7.35 (s, 1H), 7.65 (d, J=9.0 Hz, 2H), 7.77 (s, 1H), 12.68 (br s, 1H); APCI-MS (m/z) 504.11 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09000159B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-9e500648d2c24a6ab0eb7f7c07be6a04 |
| Source note | uspto-grants-2015_04 |