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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227859Generated: November 2, 2026

Diisopropylethylamine → HCID 86588362, compound

https://huagongshe.com/reaction/2227859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBoc-6-Ahx-OSuHCID 5074016—
ReactantEthyl 4-aminomethylsalicylate hydrochlorideHCID 12794728—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86588362HCID 86588362128.1%

Reaction Steps

Ethyl 4-aminomethyl-2-hydroxybenzoate hydrochloride (0.52 g, 1.28 mmoles) was suspended in anhydrous N,N-dimethylformamide (25 mL), and N,N-diisopropylethylamine (0.79 mL, 4.53 mmoles) was added, followed by N-tert-butoxycarbonyl-6-aminohexanoic acid succinimidyl ester (0.74 g, 2.26 mmoles). The mixture was stirred under dry nitrogen for 18 hours, during which time all solids dissolved. The reaction mixture was diluted with ethyl acetate (100 mL) and extracted with 1 N aqueous hydrochloric acid (100 mL). The layers were separated, and the ethyl acetate solution was washed with water (100 mL) and saturated aqueous sodium chloride (500 mL). The ethyl acetate solution was dried over anhydrous magnesium sulfate, filtered, and evaporated to afford an amorphous off-white solid. Finally, the solid was crystallized from ethyl acetate, filtered, and dried in vacuo to afford 0.67 g (73% yield) of ethyl (N-tert-butoxycarbonyl-6-aminohexanoyl)aminomethyl-2-hydroxybenzoate (m.p. 120-121° C., open capillary, uncorrected).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414122B1
Source datasetuspto-grants-2002_07
ORD IDord-0a379f216025481a9533d83fa1ed8b55
Source noteuspto-grants-2002_07