[(1S,3S)-3-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S,4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]carbamic acid tert-butyl ester

[(1S,3S)-3-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S,4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]carbamic acid tert-butyl ester

(2R,5S)-5-(4-amino-5-fluoro-2-oxo-1(2H)-pyrimidinyl)-1,3-oxathiolane-2-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester

(2R,5S)-5-(4-amino-5-fluoro-2-oxo-1(2H)-pyrimidinyl)-1,3-oxathiolane-2-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester

4-nitrobenzyl (2S,4S)-4-acetylthio-2-[[N-sulfamoyl-N-(tert-butoxycarbonyl)amino]methyl]pyrrolidine-1-carboxylate

$200.00
CAS No.: 491878-06-9
Catalog No.: 110000
Purity: 95%
MF: C20H28N4O9S2
MW: 532.597
Storage: 2-8 degree Celsius
SMILES: CC(=O)S[C@H]1C[C@@H](CN(C(=O)OC(C)(C)C)S(N)(=O)=O)N(C1)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O
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4-nitrobenzyl (2S,4S)-4-acetylthio-2-[[N-sulfamoyl-N-(tert-butoxycarbonyl)amino]methyl]pyrrolidine-1-carboxylate; CAS No.: 491878-06-9; ChemShuttle s building blocks for drug discovery include this sulfamoyl-pyrrolidine for protease inhibitor development. The Boc-protected sulfamoyl group enables controlled deprotection during synthesis. Our Mitsunobu reaction achieves complete inversion at the 4-position. The product serves as a key intermediate for HCV NS3/4A protease inhibitors, supporting antiviral drug development.

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