Morpholine → HCID 9973027, compound
Reaction equation
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[Cl:7][C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:15]2[CH:20]=[C:19](F)[N:18]=[C:17]([C:22]#[N:23])[N:16]=2)=[CH:10][CH:9]=1>C(O)(C)C>[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([NH:14][C:15]2[CH:20]=[C:19]([N:1]3[CH2:6][CH2:5][O:4][CH2:3][CH2:2]3)[N:18]=[C:17]([C:22]#[N:23])[N:16]=2)=[CH:12][CH:13]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Morpholine (0.16 g) was added to a solution of the product from step (ii) (0.16 g) in iso-propylalcohol (4 ml) and stirred for 2 h at room temperature. The mixture was partitioned between ethyl acetate and aqueous sodium hydrogencarbonate solution, the organics separated, dried (MgSO4) and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with isohexane/ethyl acetate (1:1). Yield 0.09 g
Workup
- customThe mixture was partitioned between ethyl acetate and aqueous sodium hydrogencarbonate solution
- dry with materialthe organics separated, dried (MgSO4)
- customevaporated under reduced pressure
- customThe residue was purified by chromatography on silica eluting with isohexane/ethyl acetate (1:1)
Sources & evidence
- ORD record
- ord-478c587d02a648faa862bd5736563c11
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07125881B2
Reaction notes
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