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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063991Generated: November 2, 2026

Triethylamine → HCID 22275271, compound

https://huagongshe.com/reaction/1063991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHCID 22275143HCID 22275143—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 22275271HCID 2227527197.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of acid 4-[2-(1-([(4-chlorophenyl)sulfonyl]-2,5-difluoroanilino}ethyl)phenoxy]butanoic acid (107 mg, 0.21 mmol), HOBT (31 mg, 0.23 mmol), EDCI (44 mg, 0.23 mmol), Et3N (88 μL, 0.63 mmol) and CH3NH2.HCl (16 mg, 0.23 mmol) in CH2Cl2 (1.0 mL) was stirred at 25° C. for 13 h. The mixture was diluted with ethyl acetate. The organic solution was washed with H2O and sat. NaCl solution then dried over MgSO4. Concentration and chromatography afforded the amide (107 mg, 97%) as colorless gum: Rf 0.32 (10:20, hexane-ethyl acetate); 1H NMR (CDCl3, 300 MHz) δ 7.64 (d, 2H, J=6.9 Hz), 7.42 (d, 2H, J=7.8 Hz), 7.18 (t, 1H, J=8.7 Hz), 6.36-6.91 (m, 7H), 6.26 (q, 1H, 1=6.9 Hz), 4.13 (m, 1H), 4.05 (m, 1H), 2.78 (m, 4H), 2.57 (m, 1H), 2.23 (m, 2H), 1.55 (br s, 3H); LCMS m/z 524 (M+H+, C25H25ClF2N2O4S requires 522.99).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967196B1
Source datasetuspto-grants-2005_11
ORD IDord-1f0b86dc67e0440b9424772dd145443a
Source noteuspto-grants-2005_11