Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219822Generated: October 30, 2026

Triethylamine → HCID 67542103, compound

https://huagongshe.com/reaction/219822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 3-amino-4-[isobutyl(propyl)amino]benzoateHCID 67528421—
SolventDichloromethaneHCID 6344—
ProductHCID 67542103HCID 6754210394%

Reaction Steps

To a solution of ethyl 3-amino-4-[isobutyl(propyl)amino]benzoate (5 g, 0.0179 mol) in dry DCM (50 mL) was added triethyl amine (7.24 g, 0.0716 mol) at RT. Methane sulphonyl chloride (2.67 g, 0.0233 mol) was added in drops at 0° C. The reaction mixture was stirred at RT for 4 h. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in water, extracted with ethylacetate (2×75 mL), washed with 0.5M HCl, brine, dried over sodium sulphate and evaporated to afford the title compound as a yellow oil (6 g, 93%). 1H NMR (DMSO-d6, 400 MHz) δ 8.45 (s, 1H), 7.86 (s, 1H), 7.65 (m, 1H), 7.28 (m, 1H), 4.28 (m, 2H), 3.09 (s, 3H) 3.01 (m, 2H), 2.86 (m, 2H), 1.68 (m, 1H), 1.42 (m, 2H), 1.28 (m, 3H), 0.80 (m, 9H). LC/MS (Method A): 357.0 (M+H)+. HPLC (Method B) Rt 5.09 min (purity: 94.40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202865B2
Source datasetuspto-grants-2012_06
ORD IDord-969f0eab5e264e2d87ee176d7aa7ed98
Source noteuspto-grants-2012_06