تفاعل #80559

ord-2f9f55238b704974972030b3c51a0f9a

معادلة التفاعل

CCCN(C1CCCC1)[C@H]1COc2c(F)ccc(OS(=O)(=O)C(F)(F)F)c2C1
(R)-3-(N-Cyclopentyl-N-n-propylamino)-8-fluoro-5-trifluoromethylsulfonyloxy-3,4-dihydro-2H-1-benzopyran
CCN(CC)CC
triethylamine
CO
methanol
CN(C)C=O
DMF
[C]=O
carbon monoxide
CCCN(C1CCCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
title compound
المردود 86.0%
CCCN(C1CCCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Methyl (R)-3-(N-Cyclopentyl-N-n-propylamino)-8-fluoro-3,4-dihydro-2H-1-benzopyran-5-carboxylate
المردود 86.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter evaporation of the solvent in vacuo

الإجراء التجريبي

(R)-3-(N-Cyclopentyl-N-n-propylamino)-8-fluoro-5-trifluoromethylsulfonyloxy-3,4-dihydro-2H-1-benzopyran (3.7 g, 8.7 mmol), DMF (50 mL), triethylamine (2.5 g, 25 mmol), methanol (4 g, 130 mmol), palladium(ll)acetate (100 mg, 0.45 mmol) and 1,3-bis(diphenylphosphino)propane (200 mg, 0.48 mmol) were placed in a round-bottomed flask. The solution was stirred at 75° C. in an atmosphere of carbon monoxide for 4 h. After evaporation of the solvent in vacuo and subjecting the crude to flash chromatography, 2.5 g (86% yield) of the title compound as a colorless oil was isolated. GC/MS (70 eV) M=335 (20 %).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05616610uspto-grants-1997_04