Hydrochloric Acid → 3-Amino-1-(morpholin-4-yl)propan-1-one hydrochloride

HRID 586089Notes

Reaction equation

HRID 586089 reaction equation
[N:1]1([C:7](=[O:11])[CH2:8][C:9]#[N:10])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[ClH:12]>[Pt].CO>[ClH:12].[NH2:10][CH2:9][CH2:8][C:7]([N:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1)=[O:11]

Participants

5

Conditions

Temperature
25 °C

Procedure

A nitrogen inerted reactor is charged with 5% Pt—C (43 g; 58% water-wet) followed by 3-morpholin-4-yl-3-oxo-propionitrile (2.8 mol). A solution of MeOH (3.4 L) and 12N HCl (3.08 mol) is added at such a rate as to maintain an internal temperature of ca. 25° C. The vessel and its contents are degassed via three N2 pressure purges (50 psi). The atmosphere is switched to hydrogen via three H2 pressure purges (50 psi), and the reaction is stirred vigorously at ca. 25° C. under a sustained pressure of hydrogen (50 psi) for ca. 24 hours. The H2 pressure is released and replaced with N2. The reaction is passed through filter agent, which is subsequently washed with MeOH (500 mL). The reaction is concentrated in vacuo to a volume of ca. 1.4 L, and IPA (2.2 L) is added. The reaction mixture is cooled to 0° C. and filtered. The filter cake is washed with MtBE (500 mL) and dried under vacuum at ca. 30° C. to provide 3-amino-1-morpholin-4-yl-propan-1-one, hydrochloride as a white solid (439 g). This material is used in subsequent steps without further purification.

Workup

  1. customThe vessel and its contents are degassed via three N2 pressure
  2. filtrationthrough filter agent, which
  3. washis subsequently washed with MeOH (500 mL)
  4. concentrationThe reaction is concentrated in vacuo to a volume of ca. 1.4 L, and IPA (2.2 L)
  5. additionis added
  6. temperatureThe reaction mixture is cooled to 0° C.
  7. filtrationfiltered
  8. washThe filter cake is washed with MtBE (500 mL)
  9. customdried under vacuum at ca. 30° C.

Sources & evidence

ORD record
ord-817b6ecb346a48a98de7e936f2b7e4f4
Source dataset
uspto-grants-2005_08
Patent number
US06933393B2

Reaction notes

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