Tributylstannane → HCID 178441857, compound

HRID 1654139Notes

Reaction equation

HRID 1654139 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-d06c01f66a7a4e1c90542051f70ae2e2
Source dataset
uspto-grants-1995_04
Patent number
US05405849

Reaction notes

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