تفاعل #80562

ord-3a6c3dbf6754455198e60a41e52839a2

معادلة التفاعل

CCCN(C1CCCCC1)[C@H]1COc2c(F)ccc(OS(=O)(=O)C(F)(F)F)c2C1
(R)-3-(N-Cyclohexyl-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(C1CCCCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
title compound
المردود 76.0%
CCCN(C1CCCCC1)[C@H]1COc2c(F)ccc(C(=O)OC)c2C1
Methyl (R)-3-(N-Cyclohexyl-N-n-propylamino)-8-fluoro-3,4-dihydro-2H-1-benzopyran-5-carboxylate
المردود 76.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter evaporation of the solvent in vacuo

الإجراء التجريبي

(R)-3-(N-Cyclohexyl-N-n-propylamino)-8-fluoro-5-trifluoromethylsulfonyloxy-3,4-dihydro-2H-1-benzopyran (0.8 g, 1.8 mmol) (4), DMF (30 mL), triethylamine (0.5 g, 5 mmol), methanol (0.8 g, 13 mmol), palladium(II)acetate (30 mg, 0.14 mmol) and 1,3-bis(diphenylphosphino)propane (60 mg, 0.14 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, 0.6 g (76% yield) of the title compound as a colorless oil was isolated. GC/MS (70 eV) M=349 (30 %).

المصدر

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