Morpholine → 2-Morpholinopyrimidine-5-boronic acid

HRID 626928

Reaktionsgleichung

Reaktionsgleichung von HRID 626928
Cl[C:2]1[N:7]=[CH:6][C:5]([B:8]([OH:10])[OH:9])=[CH:4][N:3]=1.[NH:11]1[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1.C(N(CC)CC)C>CCO>[N:11]1([C:2]2[N:7]=[CH:6][C:5]([B:8]([OH:10])[OH:9])=[CH:4][N:3]=2)[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1

Komponenten

5

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of 2-chloropyrimidin-5-ylboronic acid (3 g, 19.0 mmol), morpholine (1.66 mL, 19 mmol) and triethylamine (1.67 mL, 19.19 mmol) in EtOH (20 mL) was stirred at 80° C. for 5 h. LCMS indicated completion of the reaction. The reaction mixture was concentrated in vacuo and the residue was taken up in ethanol (approximately 5 mL). Diethyl ether was added, and the triethylamine hydrochloride salt that crystallised out was filtered and discarded. The filtrate was concentrated in vacuo and water (approximately 10 mL) was added. The mixture was placed in a refrigerator for 1 h, after which time the resulting solid was filtered off, washed with the minimum amount of water and dried by suction, to give the title compound (2.7 g, 68%) as an off-white solid. δH (DMSO-d6) 8.64 (s, 2H), 8.08 (s, 2H), 3.73 (m, 4H), 3.65 (m, 4H). LCMS (ES+) 210 (M+H)+, RT 0.15 minutes.

Aufarbeitung

  1. customcompletion of the reaction
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. additionDiethyl ether was added
  4. customthe triethylamine hydrochloride salt that crystallised out
  5. filtrationwas filtered
  6. concentrationThe filtrate was concentrated in vacuo and water (approximately 10 mL)
  7. additionwas added
  8. waitThe mixture was placed in a refrigerator for 1 h
  9. filtrationafter which time the resulting solid was filtered off
  10. washwashed with the minimum amount of water
  11. customdried by suction

Quellen und Nachweise

ORD-Eintrag
ord-5c52ba6cdeb14ff7836b76be3b9116a4
Quelldatensatz
uspto-grants-2016_04
Patentnummer
US09309243B2

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