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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666769Generated: October 31, 2026

Sodium Carbonate → 2-(5-(2-(Aminomethyl)-4-fluorophenoxy)-1H-indazol-1-yl)ethanol

https://huagongshe.com/reaction/1666769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium borohydrideHCID 4311764—
Reactant5-fluoro-2-(1-(2-hydroxyethyl)-1H-indazol-5-yloxy)benzonitrileHCID 44542121—
SolventMethanolHCID 887—
Product2-(5-(2-(Aminomethyl)-4-fluorophenoxy)-1H-indazol-1-yl)ethanolHCID 44542122—

Reaction Steps

To a solution of (5-fluoro-2-(1-(2-hydroxyethyl)-1H-indazol-5-yloxy)benzonitrile (1.0 g, 3.36 mmol) and NCl2.6H2O (148 mg, 0.336 mmol) in MeOH (30 mL) was added NaBH4 (636 mg, 16.8 mmol) in portions (2-3), and the reaction was stirred for 3 hours. A solution of saturated Na2CO3 (15 mL) was slowly added and the mixture was stirred for 75 minutes, during which a fine solid formed. The reaction mixture was filtered thru GF/F and the cake was washed with MeOH (20 mL). The filtrate was concentrated to about 15 mL under vacuum, isopropyl acetate (20 mL) was added, and the mixture was concentrated. To the concentrate was added isopropyl acetate (20 mL) and the mixture was stirred for 5 minutes. The phases were separated, and the organic layer was washed with 10% brine (20 mL). Citric acid (0.1 M, 20 mL) was added and the phases were vigorously mixed. The organic layer was removed and the aqueous was washed with isopropyl acetate (20 mL) and EtOAc (20 mL). To the aqueous layer was added isopropyl acetate (20 mL) and 50% NaOH (1 mL) was added. The phases were vigorously mixed and the aqueous was removed. The organic was washed with 10% brine (20 mL), dried over Na2SO4 and concentrated to 850 mg (85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044083B2
Source datasetuspto-grants-2011_10
ORD IDord-014f6fdd6e5a483c8e1c41af5c9b4f59
Source noteuspto-grants-2011_10