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(4A-S*,5-R*)-2-BENZYL-5-[N-(TERT.-BUTOXYCARBONYL)-L-TRYPTOPHYL]-AMINO-1-OXO-3-THIOXOPERHYDROPYRIDO-[1,2-C]-PYRIMIDINE

Compound with spectra: 1 NMR

(4A-S*,5-R*)-2-BENZYL-5-[N-(TERT.-BUTOXYCARBONYL)-L-TRYPTOPHYL]-AMINO-1-OXO-3-THIOXOPERHYDROPYRIDO-[1,2-C]-PYRIMIDINE
SpectraBase Compound ID 1eQxayoqJUb
InChI InChI=1S/C31H37N5O4S/c1-31(2,3)40-29(38)34-25(16-21-18-32-23-13-8-7-12-22(21)23)28(37)33-24-14-9-15-35-26(24)17-27(41)36(30(35)39)19-20-10-5-4-6-11-20/h4-8,10-13,18,24-26,32H,9,14-17,19H2,1-3H3,(H,33,37)(H,34,38)/t24-,25+,26+/m1/s1
InChIKey OVFVVPNJKQOVDQ-ZNZIZOMTSA-N
Mol Weight 575.7 g/mol
Molecular Formula C31H37N5O4S
Exact Mass 575.256626 g/mol
Enantiomer InChIKey OVFVVPNJKQOVDQ-JIMJEQGWSA-N

View Spectrum of (4A-S*,5-R*)-2-BENZYL-5-[N-(TERT.-BUTOXYCARBONYL)-L-TRYPTOPHYL]-AMINO-1-OXO-3-THIOXOPERHYDROPYRIDO-[1,2-C]-PYRIMIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(4A-R*,5-S*)-2-BENZYL-5-[N-(TERT.-BUTOXYCARBONYL)-L-TRYPTOPHYL]-AMINO-1-OXO-3-THIOXOPERHYDROPYRIDO-[1,2-C]-PYRIMIDINE
(4A-S*,5-R*)-2-BENZYL-5-[N-(TERT.-BUTOXYCARBONYL)-L-TRYPTOPHYL]-AMINO-1,3-DITHIOXOPERHYDROPYRIDO-[1,2-C]-PYRIMIDINE
(4A-R*,5-S*)-2-BENZYL-5-[N-(TERT.-BUTOXYCARBONYL)-L-TRYPTOPHYL]-AMINO-3-OXO-1-THIOXOPERHYDROPYRIDO-[1,2-C]-PYRIMIDINE
(R,R)/(S,S)-2-BENZYL-5-[N-(TERT.-BUTOXYCARBONYL)-L-TRYPTOPHYL]-AMINO-1,3-DIOXO-PERHYDROPYRROLO-[1,2-C]-PYRIMIDINE
(R,S)/(S,R)-2-BENZYL-5-[N-(TERT.-BUTOXYCARBONYL)-L-TRYPTOPHYL]-AMINO-1,3-DIOXO-PERHYDROPYRROLO-[1,2-C]-PYRIMIDINE
A21459A
[(4S)-5-[(2S)-2-[(2-amino-2-keto-ethyl)carbamoyl]pyrrolidin-1-yl]-4-[[(2S)-2-[[2-[[(2S)-2-[[(2S)-3-hydroxy-2-[[(2S)-2-[[(2S)-3-(3H-imidazol-4-yl)-2-(pyroglutamoylamino)propanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]propanoyl]amino]-3-(4-hydroxyphenyl)p
PHAKELLISTATIN_15;CYCLO-(PRO-(1)-TRP-ILE-PRO-(2)-LEU-(1)-THR-PRO-(3)-LEU-(2))
CHERIMOLACYCLOPEPTIDE-C
KAWAGUCHIPEPTIN_B
Title Journal or Book Year
5-(Tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-Based Potent and Selective CCK1 Receptor Antagonists:  Structure−Activity Relationship Studies on the Central 1,3-Dioxoperhydropyrido[1,2-c]pyrimidine Scaffold Journal of Medicinal Chemistry 2001
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