HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 86747158, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,1'-(4-Chlorobutylidene)bis(4-fluorobenzene) | HCID 76820 | — |
| Reactant | HCID 20087955 | HCID 20087955 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86747158 | HCID 86747158 | — |
Reaction Steps
14.2 g of (+)-1-[(3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)methyl]-piperazine were reacted with 13.6 g of 1,1-bis(4-fluorophenyl)-4-chlorobutane and 8 g of potassium carbonate in 100 ml of dimethyl formamide for 2 h. Water was added to the mixture and after work up, the dimaleate was prepared as previously described to obtain 11.4 g of (+)-1-[4,4-bis(4-fluorophenyl)butyl]-4-[(3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1yl)methyl]piperazine (Z)-2-butenedioate (1:2) salt. mp 200° C. The free base has an optical rotation of [α]D20 =+38.5° (c=1, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05393759 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-9cdb90e9f24446c19fdff5309133583c |
| Source note | uspto-grants-1995_02 |