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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389845Generated: October 25, 2026

Dimethylformamide → (S)-N-Boc-3-aminooctanoyl-L-threonine methyl ester

https://huagongshe.com/reaction/389845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantMethyl L-threoninate hydrochlorideHCID 2734893—
Reactant916903-29-2HCID 86625424—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
Product(S)-N-Boc-3-aminooctanoyl-L-threonine methyl esterHCID 86639874—

Reaction Steps

580 mg of (S)—N-Boc-3-aminooctanoic acid prepared in the [2], 420 mg of L-threonine methyl ester hydrochloride, 1089 mg of Bop reagent, and 333 mg of HOBt were dissolved in 4.5 mL of dehydrated DMF, 0.97 mL of triethylamine was added with stirring under cooling with ice, stirred for 30 minutes under cooling with ice, and then stirred overnight at room temperature. 70 mL of ethyl acetate was added to the reaction solution obtained, washed with 10% aqueous solution of citric acid, 4% aqueous solution of sodium hydrogencarbonate, and saturated salt solution, dried over anhydrous sodium sulfate, followed by vacuum concentration. The residue was crystallized from ethyl acetate-hexane to obtain (S)—N-Boc-3-aminooctanoyl-L-threonine methyl ester. The yield was 544 mg. Analytical values are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383547B2
Source datasetuspto-grants-2013_02
ORD IDord-9e8f46e0518440bcb05e97f50bbbebef
Source noteuspto-grants-2013_02