反应详情

tetrahydro-3-furanyl N-((1S,2R)-1-benzyl-3-(cyclopentyloxy)[(4-methoxyphenyl)sulfonyl]amino-2-hydroxypropyl)carbamate. A mixture of 2,5-dioxo-1-pyrrolidinyl[(3S)tetrahydro-3-furanyl]carbonate (13.8 mg, 0.0602 mmol, WO94/05639), N1-[(2R,3S)-3-amino-2-hydroxy-4-phenylbutyl]-N1-(cyclopentyloxy)-4-methoxy-1-benzenesulfonamide×trifluoracetic acid (Step 1, Example 48), (30 mg, 0.0547 mmol), and N,N-diisopropylethylamine (23.8 μL, 0.137 mmol) were combined at ambient temperature under an Argon atmosphere. After stirring for 18 hours, the reaction mixture was evaporated in vacuo to a residue and purified on a preparative silica gel TLC plate (20×20 cm, 500 μM) eluting with 96:4 chloroform:methanol. The product band was removed, eluted with 3:1 methylene chloride:methanol, filtered, evaporated in vacuo and dried under high vacuum to provide (3S)tetrahydro-3-furanyl N-((1S,2R)-1-benzyl-3-(cyclopentyloxy)[(4-methoxyphenyl)sulfonyl]amino-2-hydroxypropyl)carbamate (26 mg, 87%) as a foam. H1-NMR (chloroform-D3): 1.73 (m, 9H), 2.14 (m, 1H), 2.92 (m, 5H), 3.77 (m, 6H), 3.87 (s, 3H), 4.79 (bm, 2H), 5.10 (bs, 1H), 6.97 (d, 2H), 7.23 (m, 5H), 7.70 (d, 2H). MS(ESI): 571 (M+Na).

1. customwere combined at ambient temperature under an Argon atmosphere
2. customthe reaction mixture was evaporated in vacuo to a residue
3. custompurified on a preparative silica gel TLC plate (20×20 cm, 500 μM)
4. washeluting with 96:4 chloroform
5. customThe product band was removed
6. washeluted with 3:1 methylene chloride
7. filtrationmethanol, filtered
8. customevaporated in vacuo
9. customdried under high vacuum