HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Sch 28080
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-3-benzyloxypyridine | HCID 90334 | — |
| Reactant | 3-Chloro-4-oxopentanenitrile | HCID 13900236 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Sch 28080 | HCID 108137 | — |
Reaction Steps
A solution of 0.86 g. of 3-chloro-4-oxopentanonitrile, 0.92 g. of 2-amino-3-phenylmethoxypyridine and 0.5 ml. of triethylamine in 15 ml. of ethanol was stirred for 16 hours, then concentrated to remove the triethylamine and ethanol. The residue was dissolved in methylene chlorideand washed with water. The methylene chloride was concentrated and the residual oil was dissolved in 20 ml. of boiling acetonitrile, filtered, cooled, and treated with hydrogen chloride/methanol with cooling to give 0.22 g. of the desired product (m.p. 163°-166° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04450164 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-cda23162da864db180393d4694b21bf1 |
| Source note | uspto-grants-1984_05 |