HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857510Generated: October 30, 2026
Hydrazine hydrate (1:1) → 4-(4-Bromo-2-chlorophenylamino)-5-chloro-6-hydrazinonicotinic acid ethyl ester
https://huagongshe.com/reaction/857510
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid | HCID 11661217 | — |
| Reactant | 4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid ethyl ester | HCID 86596780 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 4-(4-Bromo-2-chlorophenylamino)-5-chloro-6-hydrazinonicotinic acid ethyl ester | HCID 68860744 | 36.1% |
| Product | 4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid ethyl ester | HCID 86596780 | — |
Reaction Steps
4-(4-Bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid ethyl ester (48) was prepared by standard methods from 4-(4-bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid. Hydrazine monohydrate (0.59 mL, 12.16 mmol) was added to a solution of 4-(4-bromo-2-chlorophenylamino)-5,6-dichloronicotinic acid ethyl ester (48) (1.72 g, 4.05 mmol) in N,N-dimethylacetamide (20 mL). After stirring at 90° C. for 1 hour, the reaction mixture was cooled to room temperature and diluted with EtOAc. The organic layer was washed with water and brine, dried (Na2SO4) and concentrated. Purification by flash column chromatography using the Biotage system (20:1 CH2Cl2:EtOAc) provided the desired product (49) (307 mg, 18%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07144907B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-031bbe1587c24fceaafce0f80a7cd4c8 |
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| Source note | uspto-grants-2006_12 |
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