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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054598Generated: October 31, 2026

Hydrochloric Acid → HCID 69298551, compound

https://huagongshe.com/reaction/2054598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69298516HCID 69298516—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69298551HCID 6929855195.1%

Reaction Steps

2N Sodium hydroxide solution (0.21 mL, 0.42 mmol) was added dropwise to a stirred solution of methyl-4-[1-(4-bromobenzyl)-5-chloro-1H-indol-3-yl]-4-oxo-butyrate (59 mg, 0.14 mmol) in tetrahydrofuran (5 mL) and methanol (1 mL). The clear reaction mixture was stirred at room temperature until the reaction was complete (TLC control), and then diluted with water (10 mL), and acidified to pH 3 with 2N hydrochloric acid. The reaction mixture was extracted with ethyl acetate (2×20 mL). The combined extract was washed with water, brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. Purification of the product by flash column chromatography, using 5% methanol in methylene chloride as eluent, afforded the title compound as a white solid (56 mg, 95%): Rf: 0.30 (5% methanol in dichloromethane); 1H NMR (DMSO-d6, 300 MHz) δ 12.1 (1H, br s, OH), 8.67 (1H, s, ArH), 8.13 (1H, d, J=2 Hz, ArH), 7.52 (3H, m, ArH), 7.24 (3H, m, ArH), 5.48 (2H, s, CH2N), 3.12 (2H, t, J=7 Hz, CH2CO), 2.57 (2H, t, J=7 Hz, CH2CO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329680B2
Source datasetuspto-grants-2008_02
ORD IDord-71451368f63f48e490f35fbe26e11fb6
Source noteuspto-grants-2008_02