HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropyl Ether → HCID 21438294, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | 1-Allylpiperazine | HCID 806422 | — |
| Reactant | HCID 23343641 | HCID 23343641 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21438294 | HCID 21438294 | 63.5% |
Reaction Steps
1-Allylpiperazine (6.3 g.) is added to a suspension of 6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-5-phenoxycarbonyloxy-2,3,6,7-tetrahydro-5H-1,4-oxathiino[2,3-c]pyrrole (4.56 g.) in acetonitrile (25 cc.). The temperature of the reaction mixture rises to about 25° C. After 29 hours, diisopropyl ether (50 cc.) is added and the insoluble product is filtered off and washed with diisopropyl ether (2 × 15 cc.). After drying, 5-(4-allylpiperazine-1-yl)carbonyloxy-6-(7-chloro-1,8-naphthyridin-2-yl)-7-oxo-2,3,6,7-tetrahydro-5H-1,4-oxathiino[2,3-c]pyrrole (3.1 g.), melting at 254° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04021554 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-9c4dccda4fee483987999a1c20983237 |
| Source note | uspto-grants-1977_05 |