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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580903Generated: October 29, 2026

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

https://huagongshe.com/reaction/1580903

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 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 numberUS03934008
Source datasetuspto-grants-1976_01
ORD IDord-2a60a57120e04cbd8c0d0b7df8da231a
Source noteuspto-grants-1976_01