HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-Chloro-2-ethyl-4-(2-phenyl-1,3-dioxan-5-ylamino)-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Serinol | HCID 68294 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 5-Chloro-6-ethyl-4-(1,3-dihydroxy-2-propylamino)-pyridine | HCID 15346451 | — |
| Reactant | 3,4-Dichloro-2-ethylpyridine | HCID 21708425 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Chloro-2-ethyl-4-(2-phenyl-1,3-dioxan-5-ylamino)-pyridine | HCID 9880046 | — |
Reaction Steps
2.3 g (10 mmol) of 5-chloro-6-ethyl-4-(1,3-dihydroxy-2-propylamino)-pyridine (prepared analogously to Example A from 2-amino-1,3-propanediol and 3,4-dichloro-2-ethyl-pyridine) and 5.0 g of benzaldehyde were heated with 2.1 g of p-toluenesulfonic acid hydrate in 40 ml of toluene, using a water separator, until the evolution of water had ended. Working up and purification were carried out analogously to Example A. the chromatography over silica gel (ethyl acetate) gave initially 0.6 g of trans isomer (18.8% of theory), melting point: 139-140° C., and then 2.4 g of cis isomer (75.2% of theory), melting point 119-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06281221B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-986edda2c1a54907ba8a915b5cd211e7 |
| Source note | uspto-grants-2001_08 |