Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496014Generated: October 29, 2026

Water → HCID 22324310, compound

https://huagongshe.com/reaction/496014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-NitroindoleHCID 22523—
Reactant4-Chloropyridine hydrochlorideHCID 81852—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 22324310HCID 2232431058.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-nitroindole (7.0 g, 43.2 mmol) and 4-chloropyridine hydrochloride (7.8 g, 51.8 mmol) in DMF (43 mL) was added potassium tert-butoxide (12.1 g, 108.0 mmol), portionwise. The reaction was heated at 100° C. for 48 h. The mixture was allowed to cool to room temperature and poured into water (400 mL). The resulting solid was removed by filtration and dried under vacuum. Desired compound (6.04 g, 25.3 mmol; 58% yield); 1H NMR (DMSO-d6) δ 8.76 (dd, J=1.7, 4.5, 2H), 8.68 (d, J=2.2, 1H), 8.06-8.13 (m, 2H), 7.92 (d, J=9.2, 1 H), 7.75 (dd, J=1.5, 4.6, 2H), 7.07 (dd, J=0.9, 3.5, 1H); ES MS [M+H]+=240. Step 2. Preparation of 1-(4-pyridinyl)-1H-indol-5-amine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943172B2
Source datasetuspto-grants-2005_09
ORD IDord-783c0963aead4f8d81fa659e06a28cd4
Source noteuspto-grants-2005_09