HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55490Generated: October 29, 2026
Ethyl Acetate → 6-Chloropyridine-2,3-diamine
https://huagongshe.com/reaction/55490
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 6-Chloro-3-nitropyridin-2-ylamine | HCID 2724035 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 6-Chloropyridine-2,3-diamine | HCID 10630615 | 65.5% |
Reaction Steps
A mixture of 12.0 g of 2-amino-6-chloro-3-nitropyridine, 78.0 g of tin(II) chloride dihydrate and 360 ml of a 9:1 by volume mixture of ethyl acetate and 2-methyl-2-propanol was stirred at 60° C. for 1 hour, after which 1.32 g of sodium borohydride were added at 60° C., and the mixture was stirred for 3 hours at the same temperature. At the end of this time, the reaction mixture was freed from the solvent by distillation under reduced pressure. The resulting residue was diluted with water and neutralized by adding an aqueous solution of potassium carbonate, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue thus obtained was crystallized by trituration with a mixture of ethyl acetate and hexane, to give 6.50 g of title compound, melting at 120°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624935 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-bd5d08b7c8204af5a6ce20a170ff0362 |
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| Source note | uspto-grants-1997_04 |
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