Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733665Generated: October 30, 2026

Methanesulfonic Acid → HCID 68867276, compound

https://huagongshe.com/reaction/733665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant3-BromoanilineHCID 11562—
ReactantHCID 57840771HCID 57840771—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68867276HCID 68867276—

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 7-chloro-3-methyl-4-(1-morpholin-4-yl-methanoyl)-pyrrolo[2,3-c]pyridine-1-carboxylic acid tert-butyl ester, 3-bromoaniline (56 μl), and methanesulfonic acid (33 μl) in 1,4-dioxane (2 ml) was heated under microwave conditions at 180° C. for 30 minutes. The solid mass obtained was dissolved in methanol, transferred to a round bottom flask and evaporated. The residue was dissolved in ethyl acetate and washed with 5% sodium hydrogen carbonate solution and water. The organic layer was dried (MgSO4) and evaporated to give an off-white solid. The solid was triturated with diethyl ether, filtered off and sucked dry. The solid was then dissolved in warm ethyl acetate (10 ml) and treated with a solution of 1M hydrochloric acid in diethyl ether (10 drops). The resultant solid precipitate was then filtered off, sucked dry then dried at 40° C. under vacuum to afford the title compound (58 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589206B2
Source datasetuspto-grants-2009_09
ORD IDord-8128d167f3f04bfa92f9097847838a21
Source noteuspto-grants-2009_09