HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → 12-(4-n-Butyl-1-piperazinyl)-6H-indolo[2,1-c][1,4]benzodiazepine (E)-2-butenedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 12-methylthio-6H-indolo[2,1-c][1,4]benzodiazepine | HCID 13505736 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 12-(4-n-Butyl-1-piperazinyl)-6H-indolo[2,1-c][1,4]benzodiazepine (E)-2-butenedioate | HCID 131714378 | — |
Reaction Steps
A mixture of 7.1 g of 12-methylthio-6H-indolo[2,1-c][1,4]benzodiazepine, the product of Example 1c, 6.64 g of 4-n-butyl-1-piperazine and 20 ml of xylene in a pressure bottle was heated to 240° C. for 3 hours. The reaction mixture was dissolved in EtOAc, washed with water, and dried anhydrous over Na2SO4. The crude product (after removal of solvent) was dissolved in MeOH and treated with one equivalent of fumaric acid to give a solid. Recrystallization of the fumarate salt from DMF yielded the title compound, a colorless solid, mp 197° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04547497 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-7aed139ccebf4d788d7654bf96a49045 |
| Source note | uspto-grants-1985_10 |