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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964359Generated: October 29, 2026

Stannous Chloride → Ethyl 6-amino-1H-indole-4-carboxylate

https://huagongshe.com/reaction/1964359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
ReactantHCID 57470203HCID 57470203—
SolventEthanolHCID 702—
ProductEthyl 6-amino-1H-indole-4-carboxylateHCID 5343593840%

Reaction Steps

A mixture of (E)-ethyl 2-(2-(dimethylamino)vinyl)-3,5-dinitrobenzoate (11 g, 0.037 mol) and SnCl2 (83 g, 0.37 mol) in ethanol was heated at reflux for 4 h. The mixture was concentrated to dryness and the residue was poured into water and basified using sat. aq. Na2CO3 to pH 8. The precipitated solid was filtered and the filtrate was extracted with ethyl acetate (3×100 mL). The combined extracts were washed with water (2×100 mL) and brine (150 mL), dried over Na2SO4, and concentrated to dryness. The residue was purified by column on silica gel to give ethyl 6-amino-1H-indole-4-carboxylate (3.0 g, 40%). 1HNMR (DMSO-d6) δ 10.76 (br s, 1 H), 7.11-7.14 (m, 2 H), 6.81-6.82 (m, 1 H), 6.67-6.68 (m, 1 H), 4.94 (br s, 2 H), 4.32-4.25 (q, J =7.2 Hz, 2 H), 1.35-1.31 (t, J=7.2, 3 H); MS (ESI) m/e (M+H+) 205.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415387B2
Source datasetuspto-grants-2013_04
ORD IDord-54f2f123f8cf4427a9c5adadffa6ab64
Source noteuspto-grants-2013_04