Réaction #57464
ord-6e4c77e6b9c6465a8c183cfd5f26b703
Équation de réaction
Réactifs
Réactifs
Conditions de réaction
Traitement
- 1AutreThe acid was removed in vacuo
- 2Autrethe residue was partitioned between dichloromethane and 1N sodium hydroxide
- 3AutreThe organic layer was separated
- 4Extractionthe aqueous layer was extracted again with dichloromethane
- 5SéchageThe combined organic layers were dried over anhydrous sodium sulfate
- 6Filtrationfiltered
- 7Autreevaporated in vacuo
- 8AutreThe crude product was purified on flash grade silica gel eluting with dichloromethane:methanol (98:2)
- 9workup.ADDITIONFractions containing the product
- 10Autreevaporated in vacuo
- 11Autredried under high vacuum
Mode opératoire
A mixture of tert-butyl N-[(1S,2R)-1-benzyl-4-(cyclopentyloxy)-2-hydroxy-4-(6-quinoxalinylsulfonyl)butyl]carbamate (563 mg, 1.01 mmol) and trifluoroacetic acid (5 mL) was stirred under an Argon atmosphere for 0.5 hrs. The acid was removed in vacuo and the residue was partitioned between dichloromethane and 1N sodium hydroxide. The organic layer was separated and the aqueous layer was extracted again with dichloromethane. The combined organic layers were dried over anhydrous sodium sulfate, filtered and evaporated in vacuo. The crude product was purified on flash grade silica gel eluting with dichloromethane:methanol (98:2). Fractions containing the product were combined and evaporated in vacuo and dried under high vacuum to provide (3R,4S)-4-amino-1-(cyclopentyloxy)-5-phenyl-1-(6-quinoxalinylsulfonyl)-3-pentanol as a foam (379 mg, 82%). H1-NMR (chloroform-D3): 1.66 (m, 11H), 2.51 (m, 1H), 2.86 (m, 1H), 3.07 (m, 1H), 3.23 (m, 1H), 3.32 (m, 1H), 3.84 (m, 1H), 4.90 (m, 1H), 7.20 (m, 5H), 8.16 (m, 1H), 8.28 (d, 1H), 8.70 (m, 1H), 8.99 (m, 2H). MS (ESI): 457 (M+H).