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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736390Generated: October 30, 2026

Triethylamine → HCID 11165107, compound

https://huagongshe.com/reaction/736390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-Tert-ButylanilineHCID 69861—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 22170448HCID 22170448—
SolventDimethylformamideHCID 6228—
ProductHCID 11165107HCID 11165107—

Reaction Conditions

Temperature65 °C

Reaction Steps

The product from Example 37A (37.3 mg, 0.146 mmol), 4-tert-butylaniline (28 μL, 0.18 mmol), PS-DCC (1.27 mmol/g, 0.342 g, 0.435 mmol), HOBT (20.2 mg, 0.149 mmol), and triethylamine (0.062 mL, 0.45 mmol) in DMF (1.5 mL) were combined and heated at 65° C. for 16 hours. The mixture was allowed to cool to room temperature, filtered, and the filtrate was diluted with diethyl ether (20 mL). The diethyl ether was washed with water (10 mL), brine (10 mL), dried (Na2SO4), filtered, and the filtrate concentrated under reduced pressure. The residue was purified by flash chromatography (15% ethyl acetate in hexanes) to provide the title compound as a solid. 1H NMR (300 MHz, CDCl3) δ 7.99 (d, 2H), 7.83 (br s, 1H), 7.76 (m, 1H), 7.63 (d, 2H), 7.52 (d, 2H), 7.41 (d, 2H), 6.87 (m, 1H), 1.33 (s, 9H); MS (m/z) 388.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595332B2
Source datasetuspto-grants-2009_09
ORD IDord-14aa091eb7de4ae790605fc249ec6c7f
Source noteuspto-grants-2009_09