HCID 480330, Verbindung → HCID 480337, Verbindung
Reaktionsgleichung
[O:1]1[CH2:6][CH:5]([O:7][C:8](=[O:47])[NH:9][C@@H:10]([CH2:40][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)[C@H:11]([OH:39])[CH2:12][N:13]([CH2:31][C:32]([CH3:38])([CH3:37])[CH2:33][CH2:34][C:35]#[N:36])[S:14]([C:17]2[CH:22]=[CH:21][C:20]([O:23]CC3C=CC=CC=3)=[CH:19][CH:18]=2)(=[O:16])=[O:15])[CH2:4][O:3][CH2:2]1>CO>[O:1]1[CH2:6][CH:5]([O:7][C:8](=[O:47])[NH:9][C@@H:10]([CH2:40][C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][CH:42]=2)[C@H:11]([OH:39])[CH2:12][N:13]([CH2:31][C:32]([CH3:38])([CH3:37])[CH2:33][CH2:34][C:35]#[N:36])[S:14]([C:17]2[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=2)(=[O:16])=[O:15])[CH2:4][O:3][CH2:2]1Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
{(1S,2R)-1-Benzyl-3-[(4-cyano-2,2-dimethyl-butyl)-(4-benzyloxybenzenesulfonyl)-amino]-2-hydroxy-propyl]-carbamic acid[1,3]dioxan-5-yl ester (2.2 mg, 0.003 mmol) was dissolved in methanol (1 mL). Solution was degassed with nitrogen for 5 minutes the 10% Pd/C (2 mg) was added. Reaction was pressurized with H2 (1 ATM) and stirred for 30 minutes. Catalyst removed by filtration and solvent was removed in vacuo leaving 2.0 mg (95%) of product as a colorless residue. MS(ES): 576.2 (M+1), HPLC; tR=10.39 min. (84%).
Aufarbeitung
- customSolution was degassed with nitrogen for 5 minutes the 10% Pd/C (2 mg)
- additionwas added
- customReaction
- customCatalyst removed by filtration and solvent
- customwas removed in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-aa0ddf707cd84385ae2f0521b3b86cfe
- Quelldatensatz
- uspto-grants-2003_09
- Patentnummer
- US06617350B2
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