Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21503395 | HCID 21503395 | — |
| Product | HCID 86734091 | HCID 86734091 | — |
Reaction Steps
3.3 gm (9.25 millimols) of 3-[1,2,4,5-tetrahydro-11-methyl-3H-azepino[4,5-b] quinoline-3yl]propionic acid were converted into the acid chloride with 50 ml of thionylchloride. After distilling off the excess thionyl chloride, the residue was dissolved in 100 ml of benzene, and the solution was heated at its boiling point with 3 ml (35 millimols) of morpholine for 3 hours. After filtering, the solvent was distilled off in vacuo. The residue was dissolved in 2 N sodium hydroxide, the solution was extracted with chloroform, and the chloroform phase was dried over sodium sulfate and evaporated. The evaporation residue was dissolved in hot isopropanol and acidified with isopropanolic hydrochloric acid. Upon cooling, the dihydrochloride crystallized out.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03987047 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-ae58a2e077d34b9198b3f064ce91f8cb |
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| Source note | uspto-grants-1976_10 |
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