HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947269Generated: October 26, 2026
Allyltributylstannane → HCID 178446223, compound
https://huagongshe.com/reaction/1947269
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Reactant | HCID 178446224 | HCID 178446224 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178446223 | HCID 178446223 | — |
Reaction Steps
To a solution of 4-(cyclohexylamino)-8-(3-iodobenzyl)-1-pent-4-en-1-yl-1,3,8-triazaspiro[4.5]dec-3-en-2-one (920 mg, 1.72 mmol, intermediate I.1.d.1) and trans-bis(triphenylphosphine)palladium(II) chloride (121 mg, 0.17 mmol) in degassed DMF (11.5 mL) was added allyl tri-n-butyltin (0.61 mL, 1.98 mmol) in one portion. The reaction mixture was stirred at 90° C., sealed, for 16 h, diluted with EtOAc, washed with aqueous LiCl twice, dried over sodium sulfate, concentrated in vacuo and purified by flash chromatography (90 g silica gel, EtOAc) to give the desired product. LRMS (M+1)=449.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399473B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-05a948d0015948789343865cc23e7a88 |
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| Source note | uspto-grants-2013_03 |
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