반응 #678473

ord-b1a48950e7fe4f98b8090e4d2e7b37d1

반응 방정식

CC(C)(C)OC(=O)N[C@@H](C[C@H](Cc1ccc(O)cc1)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
di-tert-butyl (4S)—N-(tert-butoxycarbonyl)-4-(4-hydroxy-benzyl)-L-glutamate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1ccc(S(=O)(=O)OC2COC(c3ccccc3)OC2)cc1
2-phenyl-1,3-dioxan-5-yl 4-methylbenzenesulfonate
CC(C)(C)OC(=O)N[C@@H](C[C@H](Cc1ccc(O[C@H]2C[C@H](OCc3ccccc3)C2)cc1)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
crude product
CC(C)(C)OC(=O)N[C@@H](C[C@H](Cc1ccc(O[C@H]2C[C@H](OCc3ccccc3)C2)cc1)C(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Di-tert-butyl (4S)-4-(4-{trans-[3-(benzyloxy)cyclobutyl]oxy}benzyl)-N-(tert-butoxycarbonyl)-L-glutamate

반응 조건

온도
100°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The reaction mixture was then filtered
  2. 2
    기타the solvent evaporated

실험 절차

To 349 mg (0.75 mmol) of di-tert-butyl (4S)—N-(tert-butoxycarbonyl)-4-(4-hydroxy-benzyl)-L-glutamate (Example 1 b) in 15 mL NA-dimethylformamide were added 138 mg (1.0 mmol) of potassium carbonate and 332 mg (1.0 mmol) of 2-phenyl-1,3-dioxan-5-yl 4-methylbenzenesulfonate (Studii si Cercetari de Chimie (1960), 8, 187-99.) and the resulting suspension was heated for 2 h at 100° C. in a microwave oven. The reaction mixture was then filtered, the solvent evaporated and the residue was taken up in DMSO. The crude product obtained in this manner was chromatographed on a PrepCon® C-18 reversed phase column using a water/acetonitrile gradient (35/65 to 0/100), and the appropriate fractions were combined and concentrated.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09238631B2uspto-grants-2016_01