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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879472Generated: October 31, 2026

Diisopropylethylamine → HCID 67153303, compound

https://huagongshe.com/reaction/1879472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantL-HomocystineHCID 439579—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 58280475HCID 58280475—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67153303HCID 6715330381.3%

Reaction Steps

To a stirred solution of 2-(3-cyano-benzyl)-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid (6.0 g, 21.4 mmol) in tetrahydrofuran (40 mL) was added 1-hydroxybenzotriazole (available from 3B Scientific Corporation, Libertyville, Ill. 60048, USA; 2.8 g, 20.72 mmol), TBTU (6.8 g, 21.18 mmol) and diisopropylethylamine (8.3 g, 64.21 mmol) simultaneously at room temperature. After 16 h of stirring at the same temperature, tetrahydrofuran was distilled off under reduced pressure. The obtained crude residue was extracted with ethyl acetate (120 mL), washed with an aqueous solution of 1N NaOH (50 mL), brine (50 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a crude mass. The crude mass was purified by silica gel column chromatography (100-200 mesh) using a gradient of 50-70% ethyl acetate/hexanes to give 2-(3-cyano-benzyl)-1,1-dioxo-1λ6-isothiazolidine-3-carboxylic acid((1S,2S,3S,5R)-2,6,6-trimethyl-bicyclo[3.1.1]hept-3-yl)-amide (7.0 g, 79.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314250B2
Source datasetuspto-grants-2012_11
ORD IDord-4629e66f9b95452ea962fc06fe9de492
Source noteuspto-grants-2012_11