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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011349Generated: October 29, 2026

Hydrochloric Acid → HCID 67314578, compound

https://huagongshe.com/reaction/1011349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-fluoro-1,3-dihydro-2H-indol-2-oneHCID 3731012—
ReactantHCID 67314944HCID 67314944—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67314578HCID 6731457810%

Reaction Steps

A solution of 5-fluoro-1,3-dihydro-indol-2-one (75 mg, 0.49 mmol) in THF (4 mL) is treated with a solution of lithium bis(trimethylsilyl)amide (0.8 mL of a 1 M solution in THF, 0.8 mmol) dropwise. The resulting solution is stirred at room temperature for 10 min. A solution of 2-(4-hydroxy-piperidin-2-ylmethyl)-7H-furo[3,4-b]pyridin-5-one (70 mg, 0.28 mmol) in THF (2 mL) is added dropwise to the reaction mixture. The resulting solution is stirred for 6 h. The reaction mixture is treated with additional lithium bis(trimethylsilyl)amide (0.3 mL of a 1 M solution in THF, 0.3 mmol) dropwise and the reaction mixture is stirred at room temperature overnight. The reaction mixture is poured into a cold aqueous 10% HCl solution (7 mL). The resulting mixture is heated to 50° C. for 1 h and then poured into 100 mL ice water. Solid NaHCO3 is carefully added to adjust the pH to 8. The aqueous layer is extracted with EtOAc (2×). The combined organic extracts are dried with Na2SO4, filtered and concentrated. The residue is purified by chromatography (silica gel, MeOH-Chloroform). The product containing fractions are concentrated to give the title compound as a yellow solid (11 mg, 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977351B2
Source datasetuspto-grants-2011_07
ORD IDord-ed24629977e34ae79db183eb6eeed92c
Source noteuspto-grants-2011_07