HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242169Generated: October 31, 2026
1,3-Dichloroacetone → 2'-Amino-6'-[({2-[(3-chloro-4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]-6-(2-hydroxyethoxy)-3,4'-bipyridine-3',5'-dicarbonitrile
https://huagongshe.com/reaction/242169
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (3-Chloro-4-fluorophenyl)thiourea | HCID 704698 | — |
| Reactant | HCID 178510485 | HCID 178510485 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2'-Amino-6'-[({2-[(3-chloro-4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]-6-(2-hydroxyethoxy)-3,4'-bipyridine-3',5'-dicarbonitrile | HCID 24752906 | — |
Reaction Steps
209 mg (0.67 mmol) of 4-fluoro-3-chlorophenylthiourea and 89 mg (0.70 mmol) of 1,3-dichloroacetone are dissolved in 5 ml of DMF, and the reaction solution is stirred at 80° C. for 3 h. After cooling, 209 mg (0.67 mmol) of the compound from example 2A and 224 mg (2.67 mmol) of sodium bicarbonate are added, and the mixture is stirred at RT for a further 20 h. The mixture is then filtered through a paper filter, and sat. sodium bicarbonate solution (5 ml) is added to the filtrate. The aqueous phase is extracted with ethyl acetate (three times, 5 ml each). The combined organic phases are dried over sodium sulphate, and the solvent is removed on a rotary evaporator.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653109B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-dab2dc9de9024257854fee9ff8b76989 |
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| Source note | uspto-grants-2014_02 |
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