HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Chloro-2-methoxy-N-(2-(1-(3-isopropylureidosulfonyl)piperidin-4-yl)ethyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 5-Chloro-2-methoxy-N-(2-(1-(3-isopropylthioureidosulfonyl)piperidin-4-yl)ethyl)benzamide | HCID 11518556 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 5-Chloro-2-methoxy-N-(2-(1-(3-isopropylureidosulfonyl)piperidin-4-yl)ethyl)benzamide | HCID 59660708 | 45.6% |
Reaction Steps
0.1 ml (1.16 mmol) of 30% strength hydrogen peroxide solution was added to a solution of 48 mg (0.1 mmol) of 5-chloro-2-methoxy-N-(2-(1-(3-isopropylthioureidosulfonyl)piperidin-4-yl)ethyl)benzamide in 2 ml of 0.5 M sodium hydroxide solution at 0° C. After the reaction mixture had been kept at 0° C. for 2 hours, 100 mg of sodium sulfite were added, and the mixture was acidified by means of 2 M hydrochloric acid. The precipitated solid was filtered off, washed with water until neutral and recrystallized from diethyl ether. 21 mg (45%) of the title compound were obtained as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586612B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-c5d38b2426d34f3a80d03774077a205c |
| Source note | uspto-grants-2013_11 |