HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189556Generated: October 30, 2026
Stannous Chloride → Ethyl 6-amino-1H-indole-4-carboxylate
https://huagongshe.com/reaction/2189556
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | HCID 76548813 | HCID 76548813 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 6-amino-1H-indole-4-carboxylate | HCID 53435938 | 40% |
Reaction Steps
A mixture of 2-(2-dimethylamino-vinyl)-3,5-dinitro-benzoic acid ethyl ester (11.3 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 with sat. Na2CO3 solution to pH 8. The precipitate was filtered off 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 chromatography on silica gel to give 6-amino-1H-indole-4-carboxylic acid ethyl ester (B-18) (3 g, 40%). 1H NMR (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). ESI-MS 205.0 m/z (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324242B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-5151099d6d1245e3829ec4edb8441446 |
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| Source note | uspto-grants-2012_12 |
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