Hydrochloric Acid → 3-(6-Amino-2-benzofuran-1(3H)-ylidene)-1,3-dihydro-2H-indol-2-one

To a solution containing oxindole (0.5 g, 3.76 mmol) in 7.5 mL DMF was added 7.51 mL of sodium hexamethyldisilazane (1.0 M in THF) over 3 min. After stirring 10 min at room temperature, a solution of 6-aminophthalide (0.672 g, 4.51 mmol) in 4.0 mL DMF was added over 3 min. The reaction was stirred for 50 min at room temperature and then poured into 4% HCl to give a yellow solid. The solid was filtered to a wet cake and then partitioned between EtOAc and saturated NaHCO3. Then the mixture was heated to dissolve the solid. The organic phase was washed with H2O, brine and then dried with Na2SO4. The solvent was removed in vacuo and the resultant solid triturated with CHCl3 to afford the title compound (445 mg, 45%) as a yellow solid.

1. stirringThe reaction was stirred for 50 min at room temperature
2. customto give a yellow solid
3. filtrationThe solid was filtered to a wet cake
4. custompartitioned between EtOAc and saturated NaHCO3
5. temperatureThen the mixture was heated
6. dissolutionto dissolve the solid
7. washThe organic phase was washed with H2O, brine
8. dry with materialdried with Na2SO4
9. customThe solvent was removed in vacuo
10. customthe resultant solid triturated with CHCl3

ORDレコード

ord-c2a7fa1e3a864aa098abed3b9d4d5688

出典データセット

uspto-grants-2003_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06541504B1