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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502553Generated: November 4, 2026

Triethylamine → HCID 11669078, compound

https://huagongshe.com/reaction/502553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN1-(benzo[d]isothiazol-3-yl)ethane-1,2-diamineHCID 16768374—
ReactantN-(tert-Butoxycarbonyl)-N-phenylglycineHCID 21905636—
SolventDichloromethaneHCID 6344—
ProductHCID 11669078HCID 1166907854.5%

Reaction Steps

A mixture of N1-(benzo[d]isothiazol-3-yl)ethane-1,2-diamine (600 mg, 3.1 mmol), N α (t-butoxycarbonyl)phenylglycine (850 mg, 3.4 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (650 mg, 3.4 mmol), 1-hydroxybenzotriazole (520 mg, 3.4 mmol) and triethylamine (950 μL, 6.8 mmol) in dichloromethane (50 mL) was allowed to stir at room temperature overnight. The reaction mixture was washed successively with 1N aqueous hydrochloric acid, saturated sodium bicarbonate solution and water, then dried over anhydrous sodium sulfate, filtered and the filtrate concentrated under reduced pressure. Purification by flash column chromatography, on silica gel, eluting with a mixture of 30% ethyl acetate in hexanes and selected fractions were combined and concentrated under reduced pressure to give (S)-tert-butyl 2-(2-(benzo[d]isothiazol-3-ylamino)ethylamino)-2-oxo-1-phenylethylcarbamate (720 mg) as a white solid. 1H NMR (300 MHz, CDCl3): 7.78 (d, 1H), 7.61 (d, 1H), 7.49 (t, 1H), 7.30 (t, 1H), 7.21 (m, 2H), 7.18 (m, 2H), 6.95 (t, 1H), 5.66 (m, 2H), 5.10 (broad s, 1H), 3.62 (m, 4H), 1.39 ppm (s, 9H). MW=427 confirmed by LC-MS, tr=13.38 min (Method Y) MH+=428.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776847B2
Source datasetuspto-grants-2010_08
ORD IDord-b0ef1e469fa64f6ea0919fcbee0633b8
Source noteuspto-grants-2010_08