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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234294Generated: October 30, 2026

p-Toluenesulfonic acid monohydrate → HCID 68685078, compound

https://huagongshe.com/reaction/2234294

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant4-Amino-3-methoxy-n-(1-methylpiperidin-4-yl)benzamideHCID 11529063—
ReactantHCID 86617547HCID 86617547—
SolventMethanolHCID 887—
Solvent4-Methyl-2-PentanolHCID 7910—
ProductHCID 68685078HCID 6868507820.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

10-chloro-2-(1-methoxypropan-2-yl)-2,6,9,11-tetrazabicyclo[5.4.0]undeca-7,9,11-trien-5-one (Intermediate 137; 35 mg, 0.13 mmol)), 4-amino-3-methoxy-N-(1-methyl-4-piperidyl)benzamide (WO06/018220; 34 mg, 0.13 mmol) and p-toluenesulphonic acid monohydrate (61 mg, 0.32 mmol) were dissolved in 4-methyl-2-pentanol (2 mL) and heated at 100° C. for 18 hrs. The reaction mixture was cooled to room temperature dissolved in MeOH and added to a 2 g SCX-2 column pre wet with MeOH (2 column volumes). Flushed with MeOH (2 column volumes) and the product eluted with 2M ammonia in MeOH. Product containing fractions were evaporated and the resultant material purified by base modified reverse phase HPLC to yield the title compound as a cream coloured solid (13 mg, 20%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709471B2
Source datasetuspto-grants-2010_05
ORD IDord-da3e425c924b4e67bb92940e2dddcba7
Source noteuspto-grants-2010_05