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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449815Generated: October 30, 2026

Water → Methyl 2-amino-3-fluorobenzoate

https://huagongshe.com/reaction/449815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 58029734HCID 58029734—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-amino-3-fluorobenzoateHCID 1943202330%

Reaction Steps

HATU (230.1 mg, 0.605 mmol) was added to a solution of 5-methoxy-2-(methylsulfonamido)benzoic acid (intermediate 9) (129.2 mg, 0.527 mmol) in 4 mL of anhydrous DMF at room temperature. After 15 min of stirring, intermediate 6 (128.4 mg, 0.403 mmol) was added followed immediately by triethylamine (0.20 mL, 1.43 mmol). Reaction mixture stirred at room temperature for 18 hours under argon. Mixture was then poured into 40 mL of H2O and extracted three times with 40 mL of ethyl acetate. The combined organic layers were washed with 80 mL Brine, dried (MgSO4), filtered, and concentrated under reduced pressure leaving a residue. Product was purified by silica gel column chromatography (0-10% Methanol in Dichloromethane) and then prep HPLC (15-100% Acetonitrile (with 0.1% trifluoroacetic acid) in water (with 0.1% trifluoroacetic acid)) to yield compound 10 (56 mg, 30%) as a white solid, trifluoroacetate salt, after lyophilization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486938B2
Source datasetuspto-grants-2013_07
ORD IDord-1b4fc08a213146b4a75e845ecb254ffb
Source noteuspto-grants-2013_07