HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-(2-Chloroethyl)theophylline → HCID 13534156, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-(2-Chloroethyl)theophylline | HCID 1882 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(5-hydroxyindol-3-yl)piperidine | HCID 12229249 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | HCID 13534156 | HCID 13534156 | 43% |
Reaction Steps
A mixture of 3.65 parts of 7-(2-chloroethyl)-3,7-dihydro-1,3-dimethyl-1H-purine-2,6-dione, 3 parts of 3-(4-piperidinyl)-1H-indol-5-ol, 4.25 parts of sodium carbonate, 0.1 parts and potassium iodide and 200 parts of 4-methyl-2-pentanone was stirred and refluxed overnight. The whole was filtered while hot and the filtrate was evaporated. The residue was suspended in 45 parts of trichloromethane and 2.4 parts of methanol. The product was filtered off, washed with 16 parts of methanol and dried, yielding 2.5 parts (43%) of 3,7-dihydro-7-[2-[4-(5-hydroxy-1H-indol-3-yl)-1-piperidinyl]ethyl]-1,3-dimethyl-1H-purine-2,6-dione; mp. 232.5° C. (compound 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04548939 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-b1feb3073dc8466e92857eab1695ff2f |
| Source note | uspto-grants-1985_10 |