HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine, 3-(4-aminobutyl)- → (Z)-5,5-bis(3-methoxyphenyl)-N-[4-(3-pyridinyl)-butyl]-2,4-pentadienamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine, 3-(4-aminobutyl)- | HCID 72927 | — |
| Reactant | (Z)-5,5-bis(3-methoxyphenyl)-2,4-pentadienoic acid 4-nitrophenyl ester | HCID 14347313 | — |
| Reactant | (E)-5,5-bis[(1,1'-Biphenyl)-4-y1]-N-[4-(3-pyridinyl)butyl]-2,4-pentadienamide | HCID 14994115 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (Z)-5,5-bis(3-methoxyphenyl)-N-[4-(3-pyridinyl)-butyl]-2,4-pentadienamide | HCID 14347335 | 39% |
Reaction Steps
As in Example 134, a solution of (Z)-5,5-bis(3-methoxyphenyl)-2,4-pentadienoic acid 4-nitrophenyl ester (1.2 g) and 3-pyridinebutanamine (0.42 g) in tetrahydrofuran (7 mL) was stirred at room temperature for 1 hour. The crude amide that had been isolated in the usual way, was contaminated with a minor amount of the (E)-isomer. The mixture was separated by HPLC (ethyl acetate) and the desired product was crystallized from ether (2×) to yield 0.48 g of (Z)-5,5-bis(3-methoxyphenyl)-N-[4-(3-pyridinyl)-butyl]-2,4-pentadienamide mp 69°-73° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788206 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-755fa6dff5f34163a855a6d4ad583cae |
| Source note | uspto-grants-1988_11 |