HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → [(3R)-hexahydro-1-methyl-2-oxo-1H-azepin-3-yl]-carbamic acid, 1,1-dimethylethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | (R)-tert-Butyl (2-oxoazepan-3-yl)carbamate | HCID 2756761 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [(3R)-hexahydro-1-methyl-2-oxo-1H-azepin-3-yl]-carbamic acid, 1,1-dimethylethyl ester | HCID 21101878 | — |
Reaction Steps
To a stirred solution of [(3R)-hexahydro-2-oxo-1H-azepin-3-yl]-carbamic acid, 1,1-dimethylethyl ester (500 mg) in THF (5 mL) at rt, KHDMS (5.26 mL, 1.0 M in THF) was added. After 30 min, CH3I (0.26 mL) was introduced. The reaction was kept at rt overnight, and then quenched with brine. The reaction mixture was extracted with EtOAc, washed with brine, and dried over Na2SO4. Concentration in vacuo afforded the crude product which was used directly for the next step reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220856B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-72db042ac0104512ab8638e01f323291 |
| Source note | uspto-grants-2007_05 |