HCID 178418573, compound → HCID 178441847, compound

HRID 1974937Notes

Reaction equation

HRID 1974937 reaction equation
[CH2:1]([C:5]1[NH:6][C:7]2[C:12]([C:13](=[O:15])[N:14]=1)=[CH:11][C:10]([CH:16]=[O:17])=[CH:9][CH:8]=2)[CH2:2][CH2:3][CH3:4].[CH3:18][Mg]Br>O1CCCC1.C(OCC)C>[CH2:1]([C:5]1[NH:6][C:7]2[C:12]([C:13](=[O:15])[N:14]=1)=[CH:11][C:10]([CH:16]([OH:17])[CH3:18])=[CH:9][CH:8]=2)[CH2:2][CH2:3][CH3:4]

Participants

5

Reactant 2

HCID 178418573HCID 178418573, compoundHCID 178441857HCID 178441857, compound

Product 1

HCID 178441847HCID 178441847, compound

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent

Conditions

Temperature
0 °C

Procedure

To a solution of 0.60 g of 2-butyl-1,4-dihydro-4-oxo-6-quinazolinecarboxaldehyde in 30 ml of dry tetrahydrofuran, cooled to-0° C. is added dropwise, 2.61 ml of a 3.OM solution of methylmagnesium bromide in diethyl ether. The reaction is stirred at 0° C. for 30 minutes and then quenched with 10 ml of aqueous ammonium chloride. After diluting with 10 ml of water, the reaction mixture is extracted with 9:1 chloroformmethanol. The combined extracts are dried with magnesium sulfate, filtered and concentrated to yield 0.64 g of the desired product. CI MASS SPEC 247(MH+).

Workup

  1. additionis added dropwise
  2. customquenched with 10 ml of aqueous ammonium chloride
  3. additionAfter diluting with 10 ml of water
  4. extractionthe reaction mixture is extracted with 9:1 chloroformmethanol
  5. dry with materialThe combined extracts are dried with magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-617c5136f1704d9f8bb46e6e546bd1b3
Source dataset
uspto-grants-1994_02
Patent number
US05284853

Reaction notes

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