HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 12852332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | HCID 12852324 | HCID 12852324 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12852332 | HCID 12852332 | 51.9% |
Reaction Steps
To 30 ml of chloroform were dissolved 3 g of 3,4-dihydro-2-p-toluenesulfonyloxymethyl-2H-(1,3)-thiazino[3,2-a]benzimidazole and 10 g of piperazine. The resultant solution was refluxed for 18 hours. The reaction mixture was cooled, added with water and then extracted with chloroform, followed by washing the chloroform layer and dried over anhydrous magnesium sulfate. Chloroform was evaporated under reduced pressure and the residue was chromatographed on silica gel and eluted with chloroform to obtain 1.2 g (Yield: 51%) of the intended product, m.p. 151°-153° C.; IR νmaxKBr cm-1 : 3600-3000, 3100-2800, 1420; Anal. Calcd. for C15H20N4S: C, 62.47; L H, 6.99; N, 19.43; S, 11.11; Found: C, 62.41; H, 7.01; N, 19.70; S, 10.88.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04450109 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-44f676704e514785b84458152be89fd7 |
| Source note | uspto-grants-1984_05 |