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tert-butyl 2-benzyl-2,7-diazaspiro[3.5]nonane-7-carboxylate synthesis

2synthesis methods
-

Yield:1206969-92-7 260 mg

Reaction Conditions:

with potassium carbonate in acetonitrile at 20; for 2 h;

Steps:

1 Example 1.2-(2-benzyl-2,7-diazaspiro[3.5]nonane-7-yl)-6-trifluoromethyl-8-nitro-4H-benzo[e][1,3]thiazin-4-one

To the tert-butyl 2,7-azaspiro[3,5]nonanee-7-carboxylate (199 mg, 0.88 mmol) at room temperatureTo a solution of acetonitrile (15 mL) was added benzyl bromide (171 mg, 1 mmol) and potassium carbonate (276 mg, 2 mmol).Stir at room temperature for 2 hours.Distilled water (30 mL) was added to the reaction mixture, and ethyl acetate (20 mL×3). There are several layers in the merger.Dry over anhydrous magnesium sulfate, concentrate,Purified by silica gel column chromatography (DCM: MeOH: NH3H2O = 200: 10: 0.2) to give a pale yellow oil (260mg).

References:

CN108530447,2018,A Location in patent:Paragraph 0086; 0087