HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 46947247, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66742610 | HCID 66742610 | — |
| Reactant | HCID 86662182 | HCID 86662182 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 46947247 | HCID 46947247 | — |
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-fluoro-3-trifluoromethylphenyl)-1,3-thiazol-2-yl]acetamide (128 mg, 0.334 mmol) in the presence of NaH (16 mg, 0.666 mmol) in dry DMF (5.0 mL) to give 75 mg of the product as an off-white solid; 1H NMR (δ ppm, DMSO-d6, 300 MHz) 3.17 (s, 3H), 3.40 (s, 3H), 5.32 (s, 2H), 6.23 (s, 1H), 7.36 (s, 1H), 7.58-7.66 (m, 1H), 7.88 (s, 1H), 8.24-8.32 (m, 2H), 12.74 (br s, 1H); APCI-MS (m/z) 480.16 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09000159B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-95acf8f4461e42499d1164252248baec |
| Source note | uspto-grants-2015_04 |