HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747761Generated: October 31, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 3-[(3S)-4-[4-[1-(benzyloxycarbonyl)-4-piperidyloxy]phenyl]-3-(t-butoxycarbonylamino)-1-butenyl]benzonitrile
https://huagongshe.com/reaction/747761
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | (3-Cyanobenzyl)triphenylphosphonium bromide | HCID 2778355 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | methyl (2S)-3-[4-[1-(benzyloxycarbonyl)-4-piperidyloxy]phenyl]-2-(t-butoxycarbonylamino)propionate | HCID 86760707 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-[(3S)-4-[4-[1-(benzyloxycarbonyl)-4-piperidyloxy]phenyl]-3-(t-butoxycarbonylamino)-1-butenyl]benzonitrile | HCID 68829267 | — |
Reaction Steps
3.87 g (7.70 mmol) of methyl (2S)-3-[4-[1-(benzyloxycarbonyl)-4-piperidyloxy]phenyl]-2-(t-butoxycarbonylamino)propionate was dissolved in 77 ml of toluene. 19.3 ml (19.3 mmol) of 1.0 M solution of diisobutylaluminum hydride in hexane was added to the obtained solution at −78° C., and they were stirred for 10 minutes. 10 ml of methanol and 20 ml of saturated aqueous solution of potassium sodium tartrate were added to the resultant mixture, and they were stirred at room temperature for additional one hour. After the treatment with ethyl acetate as the extractant in an ordinary manner, the obtained oily residue was dissolved in a mixed solvent of 30 ml of ethanol and 30 ml of tetrahydrofuran. After the addition of 3.53 g (7.70 mmol) of (3-cyanobenzyl)triphenylphosphonium bromide and 1.15 ml (7.70 mmol) of DBU at room temperature, the resultant mixture was stirred for one hour. The solvent was distilled off under reduced pressure, and the residue was purified by the silica gel column chromatography to obtain the title compound in the form of a mixture of geometrical isomers (E:Z=2:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07396844B1 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-4e06595449764e2695d12705312d0ac0 |
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| Source note | uspto-grants-2008_07 |
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