HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-(2-diethylamino-ethyl)-4-(methanesulfonylamino)-2-methoxy-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(2-diethylamino-ethyl)-4-(bismethanesulfonylamino)-2-methoxy-benzamide | HCID 66934940 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-diethylamino-ethyl)-4-(methanesulfonylamino)-2-methoxy-benzamide | HCID 16748090 | 92.2% |
Reaction Steps
150 mg (0.36 mmol) of N-(2-diethylamino-ethyl)-4-(bismethanesulfonylamino)-2-methoxy-benzamide is dissolved in 10 ml of tetrahydrofuran and mixed with 1 ml of 1N potassium hydroxide solution. It is stirred for 2 hours at room temperature. Then, the tetrahydrofuran is drawn off in a vacuum, mixed with 25 ml of saturated sodium bicarbonate solution and shaken out three times with 25 ml each of methylene chloride. The collected organic phase is dried, filtered and concentrated by evaporation, and 114 mg (91.9% of theory) of N-(2-diethylamino-ethyl)-4-(methanesulfonylamino)-2-methoxy-benzamide is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07427390B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-678bca9214434652ade6c26edceda413 |
| Source note | uspto-grants-2008_09 |