Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3,5-Diethyl 4-(2-formylphenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate | HCID 13491971 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86746312 | HCID 86746312 | — |
Reaction Steps
Pyridine hydrobromide perbromide (3.2 g) was added to a solution of 4-(2-formylphenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethylester (3.15 g) and pyridine (1.3 ml) in dicloromethane (100 ml) at 0° C. and stirred for 0.5 hours. The mixture was then cooled to -10° C., treated with dimethylamine (10.6 ml) and stirred at -10° C. for 1 hour. The solvent was evaporated and the residue taken up with ethyl acetate. The solid was filtered off and the solution evaporated to dryness to obtain a red oil, which was eluted on a silica gel column (Ethyl acetate/Petrol ether/Methanol, 7:3:1) to yield the title compound as a yellow solid (from petrol ether) (2.3 g), m.p. 115°-120° C. T.l.c. (CH2Cl2 /Methanol, 95:5) Rf. 0.38.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05162345 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-f8c0924b1447449298cf31a8d62cfab5 |
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| Source note | uspto-grants-1992_11 |
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