HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844446Generated: October 30, 2026
2-Amino-5-bromopyridine → Ethyl [(5-bromopyridin-2-yl)carbamothioyl]carbamate
https://huagongshe.com/reaction/1844446
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | Ethyl isothiocyanatoformate | HCID 85320 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl [(5-bromopyridin-2-yl)carbamothioyl]carbamate | HCID 59286274 | — |
Reaction Steps
A mixture of 5-bromopyridin-2-amine (14.7 g, 85.0 mmol) and ethoxycarbonyl isothiocyanate (11.1 g, 10.0 ml, 85.0 mmol) in dioxane (300 ml) was stirred for 18 hours at 25° C. under nitrogen atmosphere. The solvent was evaporated under reduced pressure, the solid yellow residue was diluted with ethyl acetate and washed with water and brine, the organic layer was separated, dried over magnesium sulfate, filtrated and evaporated to dryness. 26.2 g (quant.) light yellow solid. Mp.: 159-161° C. MS: m/z=304.0/305.9 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946427B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-0f9ad79cecde4d8b933f4d4f6120a5fa |
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| Source note | uspto-grants-2015_02 |
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