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ChemicalBook CAS DataBase List tert-butyl 4-(benzylaMino)azepane-1-carboxylate

tert-butyl 4-(benzylaMino)azepane-1-carboxylate synthesis

2synthesis methods
-

Yield:878630-66-1 120 mg

Reaction Conditions:

Stage #1: tert-butyl 4-oxoazepane-1-carboxylate;benzylaminewith acetic acid in methanol at 25; for 0.5 h;
Stage #2: with sodium cyanoborohydride in methanol at 0 - 25; for 1.5 h;

Steps:

3.S-27 Step 1.

AcOH (53.6 μL, 0.94 mmol, 2.0 eq) was added to a solution of tert-butyl 4-oxoazepane-1-carboxylate (100.0 mg, 0.47 mmol, 1.0 eq) and BnNH2 (61.5 μL, 0.56 mmol, 1.2 eq) in MeOH (5 mL) at 25° C. The reaction was stirred for 30 min, after which NaBH3CN (44.2 mg, 0.70 mmol, 1.5 eq) was added at 0° C. and the mixture was stirred at 25° C. for additional 1.5 h. Upon completion, the reaction was quenched by the addition of water (10 mL) and extracted with DCM (3×5 mL). The combined organic layers were dried over Na2SO4 and concentrated to give crude compound SI-48 (120.0 mg) as yellow oil, which was used in step 2 without further purification.

References:

US2020/278355,2020,A1 Location in patent:Paragraph 0387; 0494-0495