#69C;(R)-6-(HYDROXYMETHYL)-N-(PYRIDIN-3-YL)-3-[[1-(TRIFLUOROMETHYLSULFONYL)-1,2,5,6-TETRAHYDROYRIDIN-3-YL]-ETHYNYL-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMIDE
Compound with spectra: 1 NMR
![#69C;(R)-6-(HYDROXYMETHYL)-N-(PYRIDIN-3-YL)-3-[[1-(TRIFLUOROMETHYLSULFONYL)-1,2,5,6-TETRAHYDROYRIDIN-3-YL]-ETHYNYL-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMIDE](/api/compound/8U9KqarMd20.png?ph=true&h=300&w=458 "#69C;(R)-6-(HYDROXYMETHYL)-N-(PYRIDIN-3-YL)-3-[[1-(TRIFLUOROMETHYLSULFONYL)-1,2,5,6-TETRAHYDROYRIDIN-3-YL]-ETHYNYL-5,6-DIHYDROPYRIDINE-1(2H)-CARBOXAMIDE")
| SpectraBase Compound ID | 8U9KqarMd20 |
|---|---|
| InChI | InChI=1S/C20H21F3N4O4S/c21-20(22,23)32(30,31)26-10-2-3-15(12-26)5-6-16-7-8-18(14-28)27(13-16)19(29)25-17-4-1-9-24-11-17/h1,3-4,7,9,11,18,28H,2,8,10,12-14H2,(H,25,29)/t18-/m1/s1 |
| InChIKey | SUTDFSGGEZNCHY-GOSISDBHSA-N |
| Mol Weight | 470.47 g/mol |
| Molecular Formula | C20H21F3N4O4S |
| Exact Mass | 470.123561 g/mol |
| Enantiomer InChIKey | SUTDFSGGEZNCHY-SFHVURJKSA-N |
| Racemate InChIKey | SUTDFSGGEZNCHY-UHFFFAOYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
N-(TRIFLUOROMETHANESULFONYL)-1,2,3,4-TETRAHYDROQUINOLINE-6-CARBOXYLIC-ACID
3-chloro-6-methyl-N-(3-pyridinyl)-1-benzothiophene-2-carboxamide
1-(2-HYDROXY-ETHYL)-3-METHYL-2,4-(1H,3H)-QUINAZOLINE-DIONE
3-(p-Methylphenyl)-1-phenyl-1,3-Diazadihydroazulan-2(6H)-one
benzonitrile, 4-[[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]sulfonyl]-
3-Chloro-N-(3-iodophenyl)-6-methyl-1-benzothiophene-2-carboxamide
N-mesityl-2-{[6-(propionylamino)-1,3-benzothiazol-2-yl]sulfanyl}propanamide
ethanediamide, N~1~-[4-(2-benzothiazolyl)phenyl]-N~2~-[(1-ethyl-3,5-dimethyl-1H-pyrazol-4-yl)methyl]-
(E)-{9-(3-Chlorobenzylidene)-3-(3-phenyl-propyl)-3-azabicyclo[3.3.1]nonan-1-yl}methanol
4-(7-chloro-2,4-dioxo-1,4-dihydro-3(2H)-quinazolinyl)-N-cyclopentylbutanamide
| 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 |