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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401473Generated: November 3, 2026

Sulfuric Acid → HCID 53373126, compound

https://huagongshe.com/reaction/1401473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 57875950HCID 57875950—
ProductHCID 53373126HCID 53373126—

Reaction Steps

1-(8-Chloro-1,2,3,4-tetrahydro-2-methylpyrido[4,3-b]indol-5-yl)-2-(6-methylpyridin-3-yl)propan-2-ol (1 g, 2.70 mmol, 1 equiv.) was refluxed with 25% sulfuric acid (7 mL) for 2 h. The reaction mixture was cooled to 5° C. in ice-water bath. KOH (15% aqueous solution) was added dropwise to the reaction mixture until pH 9-10 was achieved. The reaction mixture was extracted with EtOAc (3×10 mL). The combined organic layer was washed with water (10 mL) followed by brine, dried over sodium sulfate and evaporated under vacuum. The crude product was purified by silica gel chromatography (100-200 mesh) using a gradient of MeOH-EtOAc (0-10%) to obtain a mixture of isomers, which were separated by HPLC. 1H NMR (CD3OD, oxalate salt) δ (ppm): 8.70 (s, 1H), 8.05 (d, 1H), 7.55 (s, 1H), 7.40 (d, 1H), 7.35 (m, 2H), 7.20 (m, 1H), 5.0 (m, 2H), 4.50 (m, 2H), 4.25 (m, 1H), 3.70 (m, 2H), 3.10 (s, 3H), 2.80 (m, 2H), 2.60 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907097B2
Source datasetuspto-grants-2014_12
ORD IDord-be4207a58d324d5daddcd14cf5417008
Source noteuspto-grants-2014_12