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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456917Generated: October 30, 2026

HCID 22668358, compound → HCID 22668284, compound

https://huagongshe.com/reaction/456917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22668358HCID 22668358—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
ProductHCID 22668284HCID 22668284—

Reaction Steps

A mixture of tert-butyl 2-(2-chloro-3-quinolinyl)-5-(hydroxymethyl)-1H-indole-1-carboxylate (7-2, 800 mg, 1.96 mmol, 1 equiv) and MnO2 (850 mg, 9.8 mmol, 5.00 equiv) in dichloromethane (100 mL) was heated at reflux for 1.5 hours. Additional NbO2 (700 mg, 8.05 mmol, 4.10 equiv) was added and heating was continued for 1 hour. The catalyst was filtered and washed with dichloromethane (100 mL). The combined filtrate was concentrated to give tert-butyl 2-(2-chloro-3-quinolinyl)-5-formyl-1H-indole-1-carboxylate (8-1) as a white foam. 1H NMR (500 MHz, CDCl3) δ 10.11 (s, 1H), 8.47 (d, 1H, J=8.8 Hz), 8.22 (s, 1H), 8.16 (d, 1H, J=1.0 Hz), 8.09 (d, 1H, J=8.6 Hz), 7.95 (dd, 1H, J=8.8, 1.7 Hz), 7.89 (d, 1H, J=8.1 Hz), 7.81 (br t, 1H, J=7.6 Hz), 7.64 (br t, 1H, J=7.5 Hz), 6.80 (s, 1H), 1.27 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186723B2
Source datasetuspto-grants-2007_03
ORD IDord-0284ce46333f45fdb2d9fd0bcd5e5937
Source noteuspto-grants-2007_03