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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037263Generated: October 30, 2026

Formic Acid → HCID 11846679, compound

https://huagongshe.com/reaction/1037263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantStannous chloride dihydrateHCID 61436—
ReactantMethyl 4-amino-5-chloro-2-methoxy-3-nitrobenzoateHCID 12097752—
ProductHCID 11846679HCID 1184667931%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of 4-amino-5-chloro-2-methoxy-3-nitro-benzoic acid methyl ester (1.00 g, 3.84 mmol, prepared as described in J. Med. Chem., 2006, 49, 4762-4766) in formic acid (10.5 mL), was added tin(II) chloride dihydrate (2.6 g, 11.5 mmol). The reaction mixture was heated at 130° C. in the microwave for 10 min. Upon cooling to RT, water was added (50 mL) and the pH of the resultant mixture was adjusted to ˜7 by careful addition of 5 M sodium hydroxide. The resultant mixture was filtered through a Celite® and sand filter cake, washing with EtOAc (5×30 mL). The organic layer was separated, dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was subjected to flash chromatography (SiO2, gradient 0 to 100% EtOAc in pentane) to afford the title compound as an off-white solid (0.29 g, 31%). LCMS (Method A): RT=3.40 min, [M+H]+=241/243.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546376B2
Source datasetuspto-grants-2013_10
ORD IDord-7238e0147ae7488bba71d1bf4b404072
Source noteuspto-grants-2013_10