Tributylvinyltin → HCID 18680066, compound
Reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:14]2[CH2:16][CH:15]2[C:17]2[CH:26]=[C:25]3[C:20]([CH2:21][CH2:22][N:23]([CH3:30])[CH:24]3[CH:27]([CH3:29])[CH3:28])=[CH:19][CH:18]=2)[CH:5]=[C:6]2[C:11]=1[CH:10]=[C:9]([C:12]#[N:13])[CH:8]=[CH:7]2.[CH2:31]([Sn](CCCC)(CCCC)C=C)[CH2:32]CC>C1(C)C=CC=CC=1.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>[CH:27]([CH:24]1[C:25]2[C:20](=[CH:19][CH:18]=[C:17]([CH:15]3[CH2:16][CH:14]3[C:4]3[CH:5]=[C:6]4[C:11](=[C:2]([CH:31]=[CH2:32])[CH:3]=3)[CH:10]=[C:9]([C:12]#[N:13])[CH:8]=[CH:7]4)[CH:26]=2)[CH2:21][CH2:22][N:23]1[CH3:30])([CH3:28])[CH3:29]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 100 °C
Procedure
A solution of Example 41A (430 mg, 0.94 mmol) in toluene (10 mL) was treated with tributyl(vinyl)stannane (298 mg, 0.94 mmol), and Pd(PPh3)4 (109 mg, 0.09 mmol), flushed with argon, sealed in a tube, and heated to 100° C. for 20 hours. The mixture was cooled to room temperature, treated with ethyl acetate (10 mL), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 10% methanol/dichloromethane to provide the desired product.
Workup
- customflushed with argon
- customsealed in a tube
- temperatureThe mixture was cooled to room temperature
- additiontreated with ethyl acetate (10 mL)
- filtrationfiltered
- concentrationconcentrated
- customThe concentrate was purified by flash column chromatography on silica gel with 10% methanol/dichloromethane
Sources & evidence
- ORD record
- ord-b719b9cb48264c4881f1f15ee922af53
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06495562B1
Reaction notes
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