HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 46947244, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86662190 | HCID 86662190 | — |
| Reactant | HCID 178434372 | HCID 178434372 | — |
| Product | HCID 46947244 | HCID 46947244 | — |
Reaction Steps
The title compound was prepared according to the general procedure (Method A) by coupling Intermediate 3 (50 mg, 0.258 mmol) with 2-bromo-N-{4-[3,5-difluoro-4-(2,2-dimethylpropoxy)phenyl]-1,3-thiazol-2-yl}acetamide (130 mg, 0.310 mmol) in the presence of NaH (15 mg, 0.375 mmol) in dry DMF (5.0 mL) to give 75 mg of the product as a white solid; 1H-NMR (δ ppm, DMSO-d6, 300 MHz) 1.01 (s, 9H), 2.29 (s, 3H), 3.16 (s, 3H), 3.59 (s, 3H), 3.80 (s, 2H), 5.25 (s, 2H), 7.12 (s, 1H), 7.63 (d, J=9.6 Hz, 2H), 7.76 (s, 1H), 12.63 (br s, 1H, exchangeable with D2O); ESI-MS (m/z) 532.18 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08623880B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-aa912d4fb17841b39fb2513ee7a0ef1c |
| Source note | uspto-grants-2014_01 |