Acetic Acid → 4-Cyclopropylmorpholine-3-carboxamide

Temperatur

70 °C

2.9 g of molecular sieve 3A, 4.3 g (72 mmol) of acetic acid, 7.6 g (43.2 mmol) of 2(1-ethoxy-cyclopropyl)oxy]trimethylsilane and 4.4 g (31.7 mmol) of sodium cyanoborohydride are added successively to 1.2 g (7.2 mmol) of morpholine-3-carboxylic acid amide hydrochloride (WO2005026156 Hennequin L. F. A. et al.) in solution in methanol (36 ml). The reaction mixture is heated at 70° C. for 3.5 hours, then cooled to room temperature and filtered. The filtrate is concentrated under reduced pressure, then the residue is taken up in dichloromethane (200 ml) and washed 3 times with an aqueous solution of NaOH (1N) (100 ml). The organic phase is dried over Na2SO4, filtered and then concentrated under reduced pressure. 0.58 g of product is obtained, in the form of a white powder. Yield 47%. Melting point 116° C. MH+: 171 (Tr: 1.03 min, condition 2).

1. temperaturecooled to room temperature
2. filtrationfiltered
3. concentrationThe filtrate is concentrated under reduced pressure
4. washwashed 3 times with an aqueous solution of NaOH (1N) (100 ml)
5. dry with materialThe organic phase is dried over Na2SO4
6. filtrationfiltered
7. concentrationconcentrated under reduced pressure

ORD-Eintrag

ord-a86fd0b35bc34d6f9c669a22b5a5f379

Quelldatensatz

uspto-grants-2014_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08623893B2