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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567250Generated: October 25, 2026

Sulfuric Acid → 4-(2-Amino)ethyloxy-9-benzyl-2-methoxycarbazole-5-carboxamide

https://huagongshe.com/reaction/567250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant9-Benzyl-4-cyanomethyloxy-2-methoxycarbazole-5-carboxamideHCID 10156913—
Reactantlithium aluminium hydride THFHCID 68718528—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Amino)ethyloxy-9-benzyl-2-methoxycarbazole-5-carboxamideHCID 2273988946%

Reaction Steps

To 1.25 ml (1.25 mmol) 1M lithium aluminum hydride/THF in 8.3 ml THF at 0° C. was added H2SO4 (34.5 μl, 0.63 mmol) dropwise over 5 min. The mixture was allowed to stir at room temperature 1 hour, then a suspension of 9-benzyl-4-cyanomethyloxy-2-methoxycarbazole-5-carboxamide (0.32 g, 0.83 mmol) in 8.3 ml THF was added dropwise at a rate which kept the temperature below 26° C. After an additional 45 minutes, the reaction was quenched with 0.32 ml 1:1 THF/H2O, 0.48 ml 13% NaOH, and finally 51 μl H2O. The reaction was diluted with EtOAc and saturated NaHCO3, and the layers separated. The organic layer was extracted with brine, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed on silica gel eluting with 9:1:0.1 CH2Cl2/MeOH/NH4OH to give the subtitled product (148 mg, 46%). MS (ES+) 390.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177440B1
Source datasetuspto-grants-2001_01
ORD IDord-e42727894f0f468986969242d006b64e
Source noteuspto-grants-2001_01