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7-BROMO-N-(TERT.-BUTYL)-4-(5-CHLOROTHIOPHENE-2-CARBONYL)-2-ISOBUTYL-2,3,4,5-TETRAHYDROBENZO-[F]-[1,4]-OXAZEPINE-5-CARBOXAMIDE

Compound with spectra: 2 NMR

7-BROMO-N-(TERT.-BUTYL)-4-(5-CHLOROTHIOPHENE-2-CARBONYL)-2-ISOBUTYL-2,3,4,5-TETRAHYDROBENZO-[F]-[1,4]-OXAZEPINE-5-CARBOXAMIDE
SpectraBase Compound ID C2Vmhb8l89R
InChI InChI=1S/C23H28BrClN2O3S/c1-13(2)10-15-12-27(22(29)18-8-9-19(25)31-18)20(21(28)26-23(3,4)5)16-11-14(24)6-7-17(16)30-15/h6-9,11,13,15,20H,10,12H2,1-5H3,(H,26,28)/t15-,20+/m0/s1
InChIKey VJGKLMOBLHKRSB-MGPUTAFESA-N
Mol Weight 527.91 g/mol
Molecular Formula C23H28BrClN2O3S
Exact Mass 526.069255 g/mol
Enantiomer InChIKey VJGKLMOBLHKRSB-QRWLVFNGSA-N

View Spectrum of 7-BROMO-N-(TERT.-BUTYL)-4-(5-CHLOROTHIOPHENE-2-CARBONYL)-2-ISOBUTYL-2,3,4,5-TETRAHYDROBENZO-[F]-[1,4]-OXAZEPINE-5-CARBOXAMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of 7-BROMO-N-(TERT.-BUTYL)-4-(5-CHLOROTHIOPHENE-2-CARBONYL)-2-ISOBUTYL-2,3,4,5-TETRAHYDROBENZO-[F]-[1,4]-OXAZEPINE-5-CARBOXAMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
o-{{3-[2,3-DIHYDRO-1,3-DIOXO-1H-BENZ[de]ISOQUINOLIN-5-YL)CARBAMOYL]-2-HYDROXY-1-NAPHTHYL}AZO}BENZOIC ACID, METHYL ESTER
APRATOXIN_D
1,2,3,4,5,6,8-Hepta-O-acetyloct-3-ulopyranose
11-BETA,13-DIHYDRODEACYLCYNAROPICRIN-DIISOBUTYRATE;3-BETA,8-ALPHA-DIISOBUTYRYLOXYGUAIA-4(15),10(14)-DIEN-1-ALPHA,5-ALPHA,6-BETA,11-BETA-H-12
4a(2H)-Isoquinolinol, 1-(2-ethoxyphenyl)octahydro-2-(2-methoxybenzoyl)-
17-ACRYLOYL-4-AZA-ANDROST-16-EN-3-ONE
TROGOPTEROID_C;8-ZETA-HYDROXY-1,15-ISOPIMARADIENE-3,23-DIONE
(R)-N-[2-Allyl-1-(tert-butyldiphenylsilyloxy)ethyl]-8-methoxy-3-oxo-1,2,3,4-tetrahydroisoquinolin-7-yl]acetamide
2-Chloroethyl 2-diazo-2-(2,3-diphenyl-1,2-dihydroisoquinolin-1-yl)acetate
(7E,9aS,11S,13S,13aS)-4-Formyl-2,3,4,5,6,8,9,9a,10,11,12,13-dodecahydro-11-methyl-8-oxo-1H-indeno[1,7a-e]azonine-11,13-diyl Diacetate
Title Journal or Book Year
Long-Range Diastereoselectivity in an Ugi Reaction: Stereocontrolled and Diversity-Oriented Synthesis of Tetrahydrobenzoxazepines European Journal of Organic Chemistry 2013
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