HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 46945045, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 53675961 | HCID 53675961 | — |
| Reactant | HCID 86762212 | HCID 86762212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 46945045 | HCID 46945045 | — |
Reaction Steps
The title compound was prepared according to the general procedure (Method A) by coupling Intermediate 2 (50 mg, 0.258 mmol) with 2-bromo-N-{4-[3-chloro-4-(2,2-dimethylpropoxy)phenyl]-1,3-thiazol-2-yl}acetamide (129 mg, 0.308 mmol) in the presence of NaH (15 mg, 0.375 mmol) in dry DMF (5.0 mL) to give 85 mg of the product as a white solid; 1H-NMR (δ ppm, DMSO-d6, 300 MHz): 1.04 (s, 9H), 2.27 (s, 3H), 3.17 (s, 3H), 3.36 (s, 3H), 3.76 (s, 2H), 5.32 (s, 2H), 6.07 (s, 1H), 7.19 (d, J=8.7 Hz, 1H), 7.62 (s, 1H), 7.82 (d, J=8.4 Hz, 1H), 7.96 (s, 1H), 12.69 (br s, 1H, exchangeable with D2O); APCI-MS (m/z) 530.26 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08623880B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-f20b5cc8ffb2487fbe1e88a9431c8eae |
| Source note | uspto-grants-2014_01 |