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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-Boc-N-methyl-4-methoxy-L-phenylalanineHCID 7016369—
ReactantN-Benzyloxycarbonyl-L-threonine phenacyl esterHCID 54036068—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductO-(tert-Butyloxycarbonyl-N,O-dimethyl-L-tyrosyl)-N-benzyloxycarbonyl-L-threonine phenacyl esterHCID 54209715—

Reaction Conditions

Temperature-30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504189
Source datasetuspto-grants-1996_04
ORD IDord-11930512da894a79b50f7e176364c371
Source noteuspto-grants-1996_04