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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068682Generated: October 30, 2026

Methanesulfonic Acid → HCID 59603090, compound

https://huagongshe.com/reaction/2068682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 59603105HCID 59603105—
SolventDichloromethaneHCID 6344—
ProductHCID 59603090HCID 59603090—

Reaction Steps

To a solution of 1-(5-(benzyloxy)benzo[d]thiazol-2-yl)-3-ethylurea I (1.20 g, 3.66 mmol) in DCM (100.0 mL) was added methanesulfonic acid (4.32 mL, 66.22 mmol) and the resulting reaction mixture was stirred at room temperature for 2 h. After the completion of reaction (TLC monitoring), the solvent was evaporated. The residue was cooled and then basified with saturated NaHCO3 solution followed by extraction with EtOAc (3×100 mL). The combined organics was washed with brine, dried (Na2SO4), filtered and concentrated to obtain the desired product (0.90 g) that was carried forward to the next step without further purification. MS: 238.10 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299065B2
Source datasetuspto-grants-2012_10
ORD IDord-eaa9e7fd523a4683b22b9f6f2aa89b85
Source noteuspto-grants-2012_10