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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971581Generated: October 30, 2026

Triethylamine → BOC-Asn-Leu-Ser-Thr-OBzl

https://huagongshe.com/reaction/971581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantWoodward's reagent KHCID 77804—
ReactantN2-((tert-Butoxy)carbonyl)-L-asparagineHCID 82035—
ReactantH-Leu-Ser-Thr-OBzl.TFAHCID 131710003—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductBOC-Asn-Leu-Ser-Thr-OBzlHCID 131710002—

Reaction Conditions

Temperature20 °C

Reaction Steps

20.8 g of BOC-Asn-OH are suspended in 208 ml of acetonitrile, mixed with 22.7 g of Woodward's Reagent K and the mixture stirred for 30 minutes at 20° C. 12.6 ml of triethylamine are then added dropwise, whilst stirring, in such a way that the internal temperature does not exceed +32° C., and the mixture is cooled to 20° C. and stirred for a further 50 minutes at this temperature. The almost clear solution is cooled to 0° C. and is mixed with a solution, also cooled to 0° C., of 39.1 g of H-Leu-Ser-Thr-OBzl.TFA and 10.5 ml of triethylamine in 257 ml of dimethylformamide. The reaction mixture, which soon solidifies, is stirred overnight at room temperature, cooled to -10° C. and stirred for a further 2 hours at -10° C. Thereafter the crystalline precipitate is filtered off and the tetrapeptide derivative is washed once with cold acetonitrile, once with ethyl acetate and three times with water until it is free of chloride. The resulting product is crystallised from 370 ml of dimethylformamide, 3.7 ml of glacial acetic acid and 370 ml of acetonitrile. Melting point 225°-226° C.; [α]D = -36° (c = 2 in dimethylformamide); Rf6 = 0.85 (on silica gel).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04159981
Source datasetuspto-grants-1979_07
ORD IDord-d7b014116a0742dda512e9efdc107583
Source noteuspto-grants-1979_07