HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235534Generated: October 30, 2026
N-Methylbenzylamine → (S)-N-Benzyl-N-methyl-2-[N-(t-butoxycarbonyl)-allylamino]-3-phenyl-propionamide
https://huagongshe.com/reaction/235534
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-(t-butoxycarbonyl)-allylamino-3-phenyl-propionic acid | HCID 12944585 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-N-Benzyl-N-methyl-2-[N-(t-butoxycarbonyl)-allylamino]-3-phenyl-propionamide | HCID 54096526 | — |
Reaction Steps
Combine (S)-2-[N-(t-butoxycarbonyl)-allylamino-3-phenyl-propionic acid (11.1 g, 36.35 mmol), and THF (360 mL). Cool to -22° C. Add N-methylmorpholine (7.09 mL, 54.53 mmol) and then stir for 10 minutes. Add isobutyl chloroformate (7.09 mL, 54.53 mmol) and stir for 30 minutes at -22° C. Add N-methyl-N-benzylamine (7.09 mL, 54.53 mmol). Allow to warm to ambient temperature and stir for 2 hours. Dilute the reaction mixture with ethyl acetate and extract with water. Separate the layers, dry the organic layer over MgSO4, filter, and evaporate in vacuo. Chromatograph on silica gel eluting with 10% ethyl acetate/hexane to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05597845 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-76178a063cb047afb67db9e8ecba3a0c |
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| Source note | uspto-grants-1997_01 |
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