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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399964Generated: November 4, 2026

Methanesulfonic Acid → 1-Ethyl-3-[5-hydroxy-7-(2-pyridyl)-1,3-benzothiazol-2-yl]urea

https://huagongshe.com/reaction/1399964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant1-[5-Benzyloxy-7-(2-pyridyl)-1,3-benzothiazol-2-yl]-3-ethyl-ureaHCID 72724617—
SolventDichloromethaneHCID 6344—
Product1-Ethyl-3-[5-hydroxy-7-(2-pyridyl)-1,3-benzothiazol-2-yl]ureaHCID 72724618—

Reaction Steps

To a stirred solution of ix (76 g, 0.187 mol) in DCM (1.7 L) was added methane sulfonic acid (270 mL, 4.17 mol) dropwise over 30 min. The mixture was stirred at RT for 3 h. The reaction was concentrated in vacuo. EtOAc (1 L) was added to the residue and this solution was poured carefully onto the crushed ice. The pH of the solution was modified to 8-9 by addition of saturated NaHCO3 solution followed by extraction with EtOAc (3×5 L). The combined organics were washed with H2O, brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue was stirred in Et2O (1.0 L) for 1 h at RT and then filtered to obtain x (57.0 g, 97%). 1H-NMR (DMSO-d6, 400 MHz): δ 1.08 (t, J=7.20 Hz, 3H), 3.20 (m, 2H), 6.86 (br s, 1H), 7.0 (s, 1H), 7.46 (s, 2H), 7.96 (m, 1H), 8.10 (m, 1H), 8.76 (m, 1H), 9.59 (br s, 1H) and 10.41 (br s, 1H). MS: 315.06 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906902B2
Source datasetuspto-grants-2014_12
ORD IDord-95bab9b866c84b148ea871c5664add77
Source noteuspto-grants-2014_12