HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Diphenylmethyl)azetidin-3-yl methanesulfonate → HCID 21836533, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate | HCID 2758716 | — |
| Reactant | 1-Piperazinesulfonamide | HCID 11252198 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21836533 | HCID 21836533 | 8.1% |
Reaction Steps
A solution of 1-diphenylmethyl-3-methanesulphonyloxyazetidine (see Preparation 54) (4.8 g, 15.1 mmol) and 1-aminosulphonylpiperazine (see Example 123(f)) (5 g) in acetonitrile (50 ml) was heated under reflux for 4 hours. The reaction was cooled and the solid filtered off and washed with acetonitrile (50 ml). The filtrate was concentrated under reduced pressure and the residue slurried in hot toluene (50 ml), cooled, the solid filtered off and washed with toluene (50 ml). The product was then further purified by slurrying in hot ethyl acetate (3 ml), cooling and filtering to give the title compound (0.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05968923 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-911af1a100ac4763a5494b3269ad23cf |
| Source note | uspto-grants-1999_10 |