HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720093Generated: October 25, 2026
Urea → O-(tert-Butyloxycarbonyl-N,O-dimethyl-L-tyrosyl)-N-benzyloxycarbonyl-L-threonine phenacyl ester
https://huagongshe.com/reaction/1720093
Participants
| Role | Name | HCID | Charge |
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| Reactant | Urea | HCID 1176 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Boc-N-methyl-4-methoxy-L-phenylalanine | HCID 7016369 | — |
| Reactant | N-Benzyloxycarbonyl-L-threonine phenacyl ester | HCID 54036068 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | O-(tert-Butyloxycarbonyl-N,O-dimethyl-L-tyrosyl)-N-benzyloxycarbonyl-L-threonine phenacyl ester | HCID 54209715 | — |
Reaction Steps
2.00 g (5.38 mmol) of (8), 1.67 g (5.4 mmol) of (9) and 70 mg (0.54 mmol) of DMAP were dissolved in 20 ml of CH2Cl2 and cooled to -30° C., and 1.13 g (5.5 mmol) of DCC were added. The mixture .was allowed to reach RT overnight, the urea was filered off, the filtrate was concentrated, the residue was taken up in ether and left to stand for 1 h, and the urea was again filtered off. Sufficiently pure peptolide (10) was obtained by filtration through silica gel with PE/EA 7/3. Yield: 3.5 g (5.28 mmol, 98%), α!D20 =28.7° (c=0.96, CHCl3)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05504189 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-11930512da894a79b50f7e176364c371 |
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| Source note | uspto-grants-1996_04 |
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