Tributylstannane → HCID 178441857, compound

HRID 486022Notes

Reaction equation

HRID 486022 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](I)=[CH:9][CH:8]=2)[CH2:2][CH2:3][CH3:4].C([SnH](CCCC)CCCC)CCC.[O:30]1CCC[CH2:31]1>CN(C)C=O.C1(C)C=CC=CC=1.[Cl-].[Na+].O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:1]([C:5]1[NH:6][C:7]2[C:12]([C:13](=[O:15])[N:14]=1)=[CH:11][C:10]([CH:31]=[O:30])=[CH:9][CH:8]=2)[CH2:2][CH2:3][CH3:4]

Participants

8

Procedure

To a solution of 1.0 g of 2-butyl-1,4-dihydro-4-oxo-6-iodo-quinazoline and 0.355 g of tetrakis(triphenylphosphine)palladium in 15 ml of tetrahydrofuran and 5 ml of N,N-dimethylformamide, heated to 55° C. under an atmosphere of carbon monoxide is added a solution of 1.40 g of tri-n-butyltin hydride in 2.5 ml of toluene over 6 hours via a syringe pump. After the addition is complete the reaction is allowed to cool to room temperature, diluted with brine and extracted with chloroform. The combined organics are concentrated in vacuo and the resulting residue triturated with ether. The precipitate is collected by filtration and purified by flash chromatography on silica gel, eluting with 1:1 ethyl acetate-hexanes to give 0.35 g of the desired product, m.p. 242°-244° C.

Workup

  1. additionAfter the addition
  2. extractionextracted with chloroform
  3. concentrationThe combined organics are concentrated in vacuo
  4. customthe resulting residue triturated with ether
  5. filtrationThe precipitate is collected by filtration
  6. custompurified by flash chromatography on silica gel
  7. washeluting with 1:1 ethyl acetate-hexanes

Sources & evidence

ORD record
ord-a5f6a5c8810540c5a50495a02594673f
Source dataset
uspto-grants-1994_03
Patent number
US05290780

Reaction notes

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