Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Morpholin-4-ylmethyl-benzoyl chloride | HCID 13748961 | — |
| Reactant | 1-Cyclopropylpiperazine dihydrochloride | HCID 21220812 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Bavisant | HCID 16061509 | — |
Reaction Steps
A 250 mL, two-neck flask fitted with an addition funnel and thermocouple probe was charged with 1-cyclopropyl-piperazine dihydrochloride (7.1 g, 0.036 mol, 1.0 eq) and toluene (70 mL) and then cooled to 0° C. Aqueous NaOH solution (1.0 M, 70 mL, 2.0 eq) was added at such a rate that the reaction temperature did not exceed 10° C. Na2CO3 powder (7.5 g, 0.071 mol, 2.0 eq) was then added to the reaction mixture. The 4-morpholin-4-ylmethyl-benzoyl chloride, prepared as in Step A above (9.8 g, 0.036 mol, 1.0 eq) was added in portions over 3 minutes, while the temperature of the reaction mixture was maintained below 5° C. The reaction mixture was then stirred for 2 hrs. The reaction mixture was filtered, the layers were separated, the aqueous layer was extracted with toluene (30 mL×2), and the combined organic layers washed with brine (30 mL) and dried over Na2SO4. The solvent was removed in vacuo to yield the title compound as a as pale yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07893257B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-02174e1573074755b6ca29a81069b238 |
|---|
| Source note | uspto-grants-2011_02 |
|---|