HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170908Generated: October 30, 2026
3-Aminopyridine → 6-bromo-2-hydroxy-N-(pyridin-3-yl)quinoline-4-carboxamide
https://huagongshe.com/reaction/2170908
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propylphosphonic anhydride | HCID 111923 | — |
| Reactant | HCID 178524624 | HCID 178524624 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-bromo-2-hydroxy-N-(pyridin-3-yl)quinoline-4-carboxamide | HCID 178522203 | — |
Reaction Steps
A solution of 6-bromo-2-hydroxyquinoline-4-carboxylic acid (9.0 g) was dissolved in dichloromethane and cooled to 0° C. 3-aminopyridine (1 eq), T3P (2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane 2,4,6-trioxide, 50% solution in ethyl acetate, 1.2 eq.), and DIPEA (diisopropylethylamine, 2.0 eq) were added. The solution was stirred at 0° C. for 30 minutes and then allowed to warm to room temperature overnight. The solution was washed with water, sat. sodium chloride, dried, and concentrated. Purification by silica gel column chromatography provided 6-bromo-2-hydroxy-N-(pyridin-3-yl)quinoline-4-carboxamide (9.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051305B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-0cf51df04c2d4bfba6f26599fa057ec2 |
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| Source note | uspto-grants-2015_06 |
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