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1H-Isoindol-1-one,4-amino-2,3-dihydro-2-methyl-(9CI) synthesis

4synthesis methods
-

Yield:682757-53-5 97%

Reaction Conditions:

with hydrogen;palladium 10% on activated carbon in ethyl acetate at 20; for 5.5 h;

Steps:

15.B Step B; Preparation of 4-amino-2,3-dihydro-2-methyl-1H-isoindol-1-one

A slurry of 2, [3-DIHYDRO-2-METHYL-4-NITRO-LH-ISOINDOL-1-ONE] (i. e. product of Step A) (0.97 g, 5.1 mmol) and 10% palladium on carbon (0.24 g) in ethyl acetate (35 mL) was hydrogenated at 45 psi (310 kPa) at room temperature for 5.5 h. The mixture was then filtered through a pad of [CELITE)] diatomaceous filter aid, and the [CELITE (E)] was extracted with ethyl acetate. The filtrate was concentrated under vacuum to give the title compound (0.81 g, 97% yield). 1H NMR [(CDC13)] : [B] 7.29 (m, 2H), 6.80 (d, 1H), 4.21 (s, 2H), 3.20 (s, [3H).]

References:

WO2004/35545,2004,A2 Location in patent:Page 42-43