HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 86700284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 86700285 | HCID 86700285 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86700284 | HCID 86700284 | — |
Reaction Steps
To a solution of (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(1-oxoisoindolin-5-yl)benzo[d]thiazol-6-yl)acetate (94 mg, 0.171 mmol) in DMF (2.0 mL) was added NaH (˜10 mg, 60% oil dispersion) at 0° C. After 15 min, iodomethane (0.016 mL, 0.256 mmol) was added and after 30 min the reaction was allowed to warm to room temperature. Satd. aqueous NH4Cl was added and the reaction was diluted with EtOAc, washed sequentially with 5% aqueous LiCl and brine. The organic layer was dried over Na2SO4, concentrated and purified by flash column chromatography on silica gel using EtOAc to provide the title compound. LCMS-ESI+: calc'd for C31H31ClN2O4S: 563.2 (M+H+); found: 563.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987250B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-59d16eea51e44664a0957755748cb068 |
| Source note | uspto-grants-2015_03 |