Morpholine → HCID 58539146, compound

HRID 1804675Notes

Reaction equation

HRID 1804675 reaction equation
[F:1][C:2]1[C:3]([NH:20][CH3:21])=[N:4][C:5]([NH:8][C:9]2[CH:17]=[CH:16][C:12]([C:13]([OH:15])=O)=[CH:11][C:10]=2[O:18][CH3:19])=[N:6][CH:7]=1.[NH:22]1[CH2:27][CH2:26][O:25][CH2:24][CH2:23]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(C(C)C)CC)(C)C>CN(C)C=O.CCOC(C)=O>[F:1][C:2]1[C:3]([NH:20][CH3:21])=[N:4][C:5]([NH:8][C:9]2[CH:17]=[CH:16][C:12]([C:13]([N:22]3[CH2:27][CH2:26][O:25][CH2:24][CH2:23]3)=[O:15])=[CH:11][C:10]=2[O:18][CH3:19])=[N:6][CH:7]=1

Participants

7

Procedure

A mixture of 100 mg 4-(5-fluoro-4-(methylamino)pyrimidin-2-ylamino)-3-methoxybenzoic acid, 47 μL morpholine, 205 mg HATU, 188 mL diisopropylethylamine in 1 mL of dimethylformamide was stirred at room temperature overnight. The reaction was checked by LCMS and found to be complete. The reaction was diluted with EtOAc, and the organic layer washed with saturated NaHCO3 and brine. The organic layer was concentrated and purified by preparative reverse phase HPLC to yield 12 mg of (4-(5-fluoro-4-(methylamino)pyrimidin-2-ylamino)-3-methoxyphenyl)(morpholino)methanone.

Workup

  1. washthe organic layer washed with saturated NaHCO3 and brine
  2. concentrationThe organic layer was concentrated
  3. custompurified by preparative reverse phase HPLC

Sources & evidence

ORD record
ord-8f7ec93d1d534279bea0b010a76c58ae
Source dataset
uspto-grants-2013_01
Patent number
US08354420B2

Reaction notes

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