Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 19705323 | HCID 19705323 | — |
| Reactant | HCID 21200576 | HCID 21200576 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19591404 | HCID 19591404 | 151.2% |
Reaction Steps
A mixture of 1.4 g of the compound obtained in step B of EXAMPLE 21 and 0.6 g of 4-benzylquinuclidine in 3 ml of DMF is heated at 80° C. for 2 hours. After cooling to RT, the reaction mixture is poured into water and extracted with AcoEt, the organic phase is washed with water, with 300 ml of 10% HCl solution and with 300 ml of saturated NaCl solution and dried over MgSO4 and the solvent is evaporated off under vacuum to give 1.35 g of the expected product after crystallization from AcOEt. M.p.=172-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05977359 |
|---|
| Source dataset | uspto-grants-1999_11 |
|---|
| ORD ID | ord-93b0b5ceb8cf45aa8dbb4f4cb20a3fab |
|---|
| Source note | uspto-grants-1999_11 |
|---|