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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403980Generated: October 31, 2026

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

https://huagongshe.com/reaction/1403980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
ReactantHCID 57470203HCID 57470203—
SolventEthanolHCID 702—
ProductEthyl 6-amino-1H-indole-4-carboxylateHCID 5343593841.3%

Reaction Steps

A mixture of (E)-ethyl 2-(2-(dimethylamino)vinyl)-3,5-dinitrobenzoate (11 g, 0.037 mot) 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, 1H), 7.11-7.14 (m, 2H), 6.81-6.82 (m, 1H), 6.67-6.68 (m, 1H), 4.94 (br s, 2H), 4.32-4.25 (q, J=7.2 Hz, 2H), 1.35-1.31 (t, J=7.2, 3H); MS (ESI) m/e (M+H+) 205.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912199B2
Source datasetuspto-grants-2014_12
ORD IDord-66c8e7a8738144d3a8928ccc61332295
Source noteuspto-grants-2014_12