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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751373Generated: October 25, 2026

Piperidine → 1-(4-tert-butylphenyl)-2-piperidin-1-yl-1H-indole-3-carboxaldehyde

https://huagongshe.com/reaction/751373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant1-(4-tert-butylphenyl)-2-chloro-1H-indole-3-carboxaldehydeHCID 86035920—
Product1-(4-tert-butylphenyl)-2-piperidin-1-yl-1H-indole-3-carboxaldehydeHCID 1134895587%

Reaction Steps

1-(4-tert-Butylphenyl)-2-chloro-1H-indole-3-carboxaldehyde is reacted with piperidine as described in Step 2 of Example 29 to afford 1-(4-tert-butylphenyl)-2-piperidin-1-yl-1H-indole-3-carboxaldehyde (87% yield) as an off-white solid. TLC (silica gel, heptane-30% ethyl acetate); Rf 0.23; ESI/MS 361 (M+H); RT 4.48 min; NMR 10.14 (1H, s); 8.11 (1H, d, J=6 Hz); 7.66 (2H, d); 7.46 (2H, d); 7.16 (2H, m); 6.91 (1H, d, J=9 Hz); 3.27 (4H, m); 1.46 (6H, m); 1.36 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405300B2
Source datasetuspto-grants-2008_07
ORD IDord-ad98b52c9799430da983e3e921a30ee1
Source noteuspto-grants-2008_07