Acetic Acid → 4-Cyclopropylmorpholine-3-carboxamide

HRID 2088866ノート

反応式

HRID 2088866 の反応式
Cl.[NH:2]1[CH2:7][CH2:6][O:5][CH2:4][CH:3]1[C:8]([NH2:10])=[O:9].[C:11](O)(=O)[CH3:12].[C:15]([BH3-])#N.[Na+]>CO>[CH:12]1([N:2]2[CH2:7][CH2:6][O:5][CH2:4][CH:3]2[C:8]([NH2:10])=[O:9])[CH2:11][CH2:15]1

参加物

5

反応条件

温度
70 °C

実験手順

To 1.2 g (7.2 mmol) of morpholine-3-carboxamide hydrochloride (a synthesis of which is described in WO-2005/026 156, Hennequin L. F. A. et al.) dissolved in methanol (36 ml) are successively added 2.9 g of 3 Å molecular sieves, 4.3 g (72 mmol) of acetic acid, 7. g (43.2 mmol) of 2-[(1-ethoxycyclopropyl)oxy]trimethylsilane and 4.4 g (31.7 mmol) of sodium cyanoborohydride. The reaction mixture is heated at 70° C. for 3 hours 30 minutes, and then cooled to room temperature and filtered. The filtrate is concentrated under reduced pressure and the residue is then taken up in dichloromethane (200 ml) and washed three times with aqueous NaOH solution (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+: 171.2 (tr: 1.03 min., condition 1).

後処理

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

出典と根拠

ORDレコード
ord-aec08d966e864370b0f77c65e3762a5a
出典データセット
uspto-grants-2013_05
特許番号
US08436011B2

反応ノート

読み込み中…