Morpholine → HCID 11681118, compound

HRID 1170856Notes

Reaction equation

HRID 1170856 reaction equation
C1(C)C=CC(S([O-])(=O)=[O:8])=CC=1.[C:12]1([N:18]2[C:26]3[CH2:25][CH2:24][CH2:23][C:22](=[CH:27][CH2:28][N+:29]4[CH:34]=[CH:33]C=[CH:31][CH:30]=4)[C:21]=3[CH:20]=[N:19]2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.N1CCOCC1>C(#N)C.C(OCC)(=O)C>[N:29]1([CH2:28]/[CH:27]=[C:22]2/[C:21]3[CH:20]=[N:19][N:18]([C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=4)[C:26]=3[CH2:25][CH2:24][CH2:23]/2)[CH2:34][CH2:33][O:8][CH2:31][CH2:30]1

Participants

5

Reactant 2

HCID 8083MorpholineHCID 74017985HCID 74017985, compound

Product 1

HCID 11681118HCID 11681118, compoundYield 57.1%

Reagents, catalysts & solvents 2

HCID 6342AcetonitrileSolventHCID 8857Ethyl AcetateSolvent

Procedure

A mixture of 1-[2-(1-phenyl-1,5,6,7-tetrahydro-indazol-4-ylidene)-ethyl]-pyridinium toluene-4-sulfonate (290 mg, 0.63 mmol) and morpholin (180 mg, 1.5 mmol) in 15 mL of acetonitrile is refluxed during 4 hours, following the reaction by TLC. The solvent is next evaporated, the crude is diluted in ethyl acetate and washed three times with water. Then the organic phase is evaporated under reduced pressure. The crude thus obtained is purified by silica gel cgromatography giving (E)-4,5,6,7-tetrahydro-4-(2-(morpholin-4-yl)ethylidene)-1-phenyl-1H-indazole (110 mg, 0.36 mmol, 57%, beige solid, m.p=114-116° C.).

Workup

  1. temperatureis refluxed during 4 hours
  2. customthe reaction by TLC
  3. washwashed three times with water
  4. customThen the organic phase is evaporated under reduced pressure
  5. customThe crude thus obtained
  6. customis purified by silica gel

Sources & evidence

ORD record
ord-af72267ef291466ab6e4bd39367d3087
Source dataset
uspto-grants-2010_11
Patent number
US07829559B2

Reaction notes

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