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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226188Generated: October 25, 2026

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

https://huagongshe.com/reaction/226188

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 δH (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 numberUS07557140B2
Source datasetuspto-grants-2009_07
ORD IDord-4e436ad7cb194953aeedce217d8951c2
Source noteuspto-grants-2009_07