#71C;(2R,6R)-6-(HYDROXYMETHYL)-N-(PYRIDIN-3-YL)-2-[[(S)-1-(TRIFLUOROMETHYLSULFONYL)-1,2,5,6-TETRAHYDROPYRIDIN-2-YL]-METHYL]-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMI
Compound with spectra: 1 NMR
![#71C;(2R,6R)-6-(HYDROXYMETHYL)-N-(PYRIDIN-3-YL)-2-[[(S)-1-(TRIFLUOROMETHYLSULFONYL)-1,2,5,6-TETRAHYDROPYRIDIN-2-YL]-METHYL]-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMI](/api/compound/7vy8kVSElfr.png?ph=true&h=300&w=458 "#71C;(2R,6R)-6-(HYDROXYMETHYL)-N-(PYRIDIN-3-YL)-2-[[(S)-1-(TRIFLUOROMETHYLSULFONYL)-1,2,5,6-TETRAHYDROPYRIDIN-2-YL]-METHYL]-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMI")
| SpectraBase Compound ID | 7vy8kVSElfr |
|---|---|
| InChI | InChI=1S/C19H23F3N4O4S/c20-19(21,22)31(29,30)25-10-2-1-6-15(25)11-16-7-3-8-17(13-27)26(16)18(28)24-14-5-4-9-23-12-14/h1,3-7,9,12,15-17,27H,2,8,10-11,13H2,(H,24,28)/t15-,16+,17-/m1/s1 |
| InChIKey | FEEWOAVALVRVBG-IXDOHACOSA-N |
| Mol Weight | 460.47 g/mol |
| Molecular Formula | C19H23F3N4O4S |
| Exact Mass | 460.139211 g/mol |
| Enantiomer InChIKey | FEEWOAVALVRVBG-BBWFWOEESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(2S,8S)-2-[2'-(4'',4''-Diethoxybutyl)-N-(nosylamino)but-3'-enyl]-N'-nosyl-1,2,5,6-tetrahydropyridine
(+)-Lemannine (12,13-Dehydromatrine)
4(1H)-quinazolinone, 3-(3-chloro-4-methylphenyl)-2,3-dihydro-2,2-dimethyl-
3-Benzoyl-2-(phenylcarbamoyl)-2-azabicyclo[2.2.1]hept-5-ene
#63C;(S)-3-[[5-[4-(HYDROXYMETHYL)-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-PYRROL-3-YL]-ETHYNYL]-N-(PYRIDIN-3-YL)-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMI
[(1R,4S)-N-(But-3''-enyl)-N'-(4'',4''-diethoxybutyl)-N,N'-dinosylcyclopent-4-ene-1,3-diamine
(1S,4S)-N-(But-3''-enyl)-N'-(4'',4''-diethoxybutyl)-N,N'-dinosylcyclopent-4-ene-1,3-diamine
3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolecarboxylic acid, o-piperidinophenyl ester
(2R,6R)-6-[(2R)-2-acetoxybut-3-enyl]-1-tosyl-3,6-dihydro-2H-pyridine-2-carboxylic acid methyl ester
(8alpha,9R)-10,11-dihydrocinchonan-9-ol
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of skeletally diverse alkaloid-like molecules: exploitation of metathesis substrates assembled from triplets of building blocks | Beilstein Journal of Organic Chemistry | 2013 |