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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766284Generated: November 2, 2026

Pyridine → HCID 11314988, compound

https://huagongshe.com/reaction/1766284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Chloro-2-methylbenzenesulfonyl chlorideHCID 522734—
ReactantMethyl 5-aminobenzofuran-2-carboxylateHCID 10845388—
SolventDichloromethaneHCID 6344—
ProductHCID 11314988HCID 1131498877%

Reaction Steps

To a solution of 3-chloro-2-methylbenzenesulphonyl chloride (99 mg, 0.44 mmol) in dichloromethane (3 mL) was added pyridine (85 μL, 1.05 mmol) and the mixture was stirred under N2 for 5 min, after which time 5-amino-benzofuran-2-carboxylic acid methyl ester (80 mg, 0.42 mmol) was added. The resulting mixture was stirred for 2 h at room temperature, then saturated NaHCO3 solution (10 mL) was added and the mixture was extracted into ethyl acetate (15 mL). The organic phase was washed with brine, dried (Na2SO4), filtered and evaporated to give a residue that was purified using flash chromatography to afford an off-white solid (122 mg, 77%), single spot at Rf 0.47 (2:1 hexane:ethyl acetate). mp 139.4-140.1° C., HPLC purity 99+% (tR 1.90 min in 10% water-acetonitrile). 1H NMR (CDCl3): δ 7.83 (1H, d, J=7.9 Hz), 7.55 (1H, d, J=7.9 Hz), 7.44 (1H, d, J=9.0 Hz), 7.42 (1H, s), 7.39 (1H, d, J=2.2 Hz), 7.17 (1H, t, J=8.0 Hz), 7.05 (1H, dd, J8.7, 2.2 Hz), 6.65 (1H, s, N—H), 3.95 (3H, s), 2.72 (3H, s). LCMS: 378.16. FAB-MS (MH+, C17H14ClNO5S): calcd 379.0281, found 379.0281.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230020B2
Source datasetuspto-grants-2007_06
ORD IDord-74fa08342bce435caca367847e32c235
Source noteuspto-grants-2007_06