HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917023Generated: October 28, 2026
Chloroacetaldehyde → HCID 21866982, compound
https://huagongshe.com/reaction/917023
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | HCID 68859908 | HCID 68859908 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21866982 | HCID 21866982 | 33% |
Reaction Steps
Chloroacetaldehyde (12 μL, 0.188 mmol) was added to a mixture of 6-amino-4-(4-bromo-2-chlorophenylamino)-nicotinic acid tert-butyl ester (42) (50 mg, 0.125 mmol) in EtOH (630 μL). After stirring the reaction mixture at 80° C. for 5 hours, an additional 12 μL of chloroacetaldehyde were added and heating was continued for 10 hours. The reaction mixture was cooled to room temperature and diluted with EtOAc to give a cloudy semi-solution. The organic layer was washed with water, saturated NaHCO3 and brine. The organic layer contains a precipitate, which was collected by filtration to give the desired product (43) (15 mg, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07271178B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-e79fe4195f124c5c988f0b8e6bda03b5 |
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| Source note | uspto-grants-2007_09 |
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