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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197525Generated: November 2, 2026

Hydrochloric Acid → 4-Amino-5-(4-amino-3-fluorophenyl)pyrrolo[2,1-f][1,2,4]triazine-6-carboxylic acid

https://huagongshe.com/reaction/2197525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57758181HCID 57758181—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-5-(4-amino-3-fluorophenyl)pyrrolo[2,1-f][1,2,4]triazine-6-carboxylic acidHCID 5954919399.5%

Reaction Conditions

Temperature65 °C

Reaction Steps

1 N aqueous sodium hydroxide (253 mL, 253 mmol) was added to a suspension of ethyl 4-amino-5-(4-amino-3-fluorophenyl)pyrrolo[2,1-f][1,2,4]triazine-6-carboxylate (40.0 g, 127 mmol) in THF (400 mL) and ethanol (400 mL). The reaction mixture was heated (65° C.) for 16 h and then cooled to rt. Hydrogen chloride (4 N in 1,4-dioxane, 70 mL, 280 mmol) was added and the volatiles were removed under reduced pressure. The residue was washed with water (200 mL) and then triturated with acetone and diethyl ether to give the desired product (36.3 g 99%) containing trace impurities. 1H NMR (300 MHz, DMSO-d6) δ 12.20-12.30 (br s, 1H), 8.03 (s, 1H), 7.94-8.05 (br s, 1H), 7.89 (s, 1H), 7.02 (dd, J=12.4, 2.0 Hz, 1H), 6.73-6.92 (m, 2H), 5.22-5.47 (br s, 1H), 5.12-5.25 (br s, 1H); ES-MS m/z 288.0 (MH)+; HPLC RT (Method A) 1.13 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338594B2
Source datasetuspto-grants-2012_12
ORD IDord-cedcd71161164640a1e883ee37db3e77
Source noteuspto-grants-2012_12