3-Methylmorpholine → 5-(3-Methylmorpholino)-2-morpholinopyridin-3-amine

HRID 1431524Notes

Reaction equation

Br[C:2]1[CH:3]=[C:4]([NH2:14])[C:5]([N:8]2[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)=[N:6][CH:7]=1.C1(P(C2CCCCC2)C2C=CC=CC=2C2C(C(C)C)=CC(C(C)C)=CC=2C(C)C)CCCCC1.[CH3:49][CH:50]1[CH2:55][O:54][CH2:53][CH2:52][NH:51]1.[Li+].C[Si]([N-][Si](C)(C)C)(C)C>C1COCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].O>[CH3:49][CH:50]1[N:51]([C:2]2[CH:3]=[C:4]([NH2:14])[C:5]([N:8]3[CH2:13][CH2:12][O:11][CH2:10][CH2:9]3)=[N:6][CH:7]=2)[CH2:52][CH2:53][O:54][CH2:55]1

Participants

Conditions

Temperature: 65 °C

Procedure

To a stirred solution of 5-bromo-2-morpholinopyridin-3-amine (0.5 g, 1.94 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (0.074 g, 0.16 mmol), Pd2dba3 (0.071 g, 0.08 mmol) and 3-methylmorpholine (0.98 g, 9.7 mmol) in THF (3.9 mL). To this mixture was added LHMDS in THF (1.0 M, 10.65 mL, 10.65 mmol) and the resulting reaction was heated to 65° C. The reaction was stirred for 2.25 h. After which, the reaction was cooled to rt and then poured into water (50 mL) and extracted with EtOAc (2×50 mL) and DCM (2×50 mL). The combined organic layers were dried over magnesium sulfate and the crude product was purified on basic alumina (0-100% EtOAc/hexane) to give 5-(3-methylmorpholino)-2-morpholinopyridin-3-amine. Mass Spectrum (ESI) m/e=279.2 (M+1).

Workup

customthe resulting reaction
temperatureAfter which, the reaction was cooled to rt
extractionextracted with EtOAc (2×50 mL) and DCM (2×50 mL)
dry with materialThe combined organic layers were dried over magnesium sulfate
customthe crude product was purified on basic alumina (0-100% EtOAc/hexane)

Sources & evidence

ORD record: ord-19230917c8d04d4d98110c960c62ec92
Source dataset: uspto-grants-2015_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08940724B2

Reaction notes

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