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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217711Generated: October 25, 2026

Triethylamine → 6-(Pyridine-3-sulfonylamino)hexanoic acid methyl ester

https://huagongshe.com/reaction/2217711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 6-aminohexanoate hydrochlorideHCID 11499324—
ReactantPyridine-3-sulfonyl chloride hydrochlorideHCID 12571517—
SolventAcetonitrileHCID 6342—
Product6-(Pyridine-3-sulfonylamino)hexanoic acid methyl esterHCID 2078048976.1%

Reaction Steps

Pyridine-3-sulfonyl chloride hydrochloride (92c) (1.8 g, 5.0 mmol) was added to a solution of methyl 6-aminohexanoate hydrochloride (91) (1.82 g, 10 mmol) and triethylamine (3.03 g, 30 mmol) in acetonitrile (30 ml). The mixture was stirred for 1 hour at ambient temperature, filtered and solvents were removed under reduced pressure. The oily product was dissolved in water (15 ml) and extracted with ethyl ether (50 ml). The extract was dried (Na2SO4) and the solvents were removed under reduced pressure. The title compound (1.09 g, 76%) was obtained as oil and was used for the next step without an additional purification. 1H NMR 5H (90 MHz, DMSO-d6) δ: 0.80-1.51 (6H, m, CH2); 1.83 (2H, t, J=6.5 Hz, CH2); 2.76 (2H, t, J=6.5 Hz, CH2N); 3.58 (3H, s, CH3); 7.54 (1H, dd, J=5.0 Hz, J=8.2 Hz, C5HN); 8.12 (1H, dt, J=2.0 Hz, J=8.2 Hz, C5HN); 8.61 (1H, dd, J=2.0 Hz, J=5.0 Hz, C5HN); 8.81 (1H, d, J=2.0 Hz, C5HN).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407988B2
Source datasetuspto-grants-2008_08
ORD IDord-10b1d605a31e4f2e80dcb447065e860a
Source noteuspto-grants-2008_08