HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 86662196, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66742610 | HCID 66742610 | — |
| Reactant | HCID 86662197 | HCID 86662197 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86662196 | HCID 86662196 | — |
Reaction Steps
The title compound was prepared according to the general procedure (Method A) by coupling Intermediate 1 (50 mg, 0.110 mmol) with 2-bromo-N-{4-[3,5-dichloro-4-(2,2-dimethylpropoxy)phenyl]-1,3-thiazol-2-yl}acetamide (23 mg, 0.128 mmol) in the presence of NaH (7 mg, 0.291 mmol) in dry DMF (5.0 mL) to give 30 mg of the product as an off-white solid; 1H NMR (δ ppm, DMSO-d6, 300 MHz) 1.08 (s, 9H), 3.17 (s, 3H), 3.39 (s, 3H), 3.67 (s, 2H), 5.32 (s, 2H), 6.22 (s, 2H), 7.35 (s, 1H), 7.85 (s, 1H), 8.00 (s, 2H), 12.68 (br s, 1H); APCI-MS (m/z) 550.20 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09000159B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-703d9d1bb3ab45bea15a5d00f9c2c652 |
| Source note | uspto-grants-2015_04 |