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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472929Generated: October 30, 2026

Sodium Hydroxide → HCID 67216304, compound

https://huagongshe.com/reaction/472929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67215851HCID 67215851—
SolventMethanolHCID 887—
ProductHCID 67216304HCID 67216304—

Reaction Conditions

Temperature70 °C

Reaction Steps

1.4 ml of a 1N aqueous sodium hydroxide solution are added to 0.34 g (0.7 mmol) of methyl 3-(3-{3-methoxy-4-[(propylsulfonyl)amino]benzoyl}imidazo[1,5-a]pyridin-1-yl)benzoate obtained in example 190 in 20 ml of methanol. The reaction medium is heated at 70° C. for 3 hours and then concentrated under reduced pressure. The residue is taken up in water and the aqueous phase obtained is washed with dichloromethane, neutralized by addition of 1.4 ml of 1N hydrochloric acid and then extracted with dichloromethane. The organic phase obtained is dried over sodium sulfate and concentrated under reduced pressure. 0.19 g of a yellow solid is collected, which solid is salified in the sodium salt.2.1H2O form. Melting point: 145° C.; 1H NMR (d6-DMSO): 0.96-1.01 (3H, t), 1.71-1.83 (2H, m), 3.16-3.19 (2H, m), 4.00 (3H, s), 7.33-7.70 (2H, m), 7.36-7.38 (1H, m), 7.52-7.97 (2H, m), 8.04-8.07 (2H, m), 8.27-9.85 (2H, m), 8.44 (1H, s), 8.64 (1H, s), 9.25 (1H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633216B2
Source datasetuspto-grants-2014_01
ORD IDord-efc8da5f9e2a4abc9901ab3ec27861eb
Source noteuspto-grants-2014_01