HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415495Generated: October 28, 2026
4-chloroquinolin-3-amine → HCID 86625942, compound
https://huagongshe.com/reaction/415495
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-chloroquinolin-3-amine | HCID 817332 | — |
| Reactant | 4-Chloro-1,5-naphthyridin-3-amine | HCID 66619961 | — |
| Product | HCID 86625942 | HCID 86625942 | — |
| Product | HCID 86625943 | HCID 86625943 | — |
Reaction Steps
In step (1) of Reaction Scheme I, a 4-chloroquinolin-3-amine or 4-chloro[1,5]naphthyridin-3-amine of Formula XX is reacted with an acid halide of Formula Hal-Z—CH2—C(O)—Hal to provide an N-(4-chloroquinolin-3-yl)amide or N-(4-chloro[1,5]naphthyridin-3-yl)amide of Formula XXI. The reaction can be carried out by heating a solution of a compound of Formula XX and the acid halide in a suitable solvent such as 1,2-dichloroethane. Some acid chlorides of Formula Hal-Z—CH2—C(O)—Hal are commercially available; others can be prepared using conventional synthetic methods. Some 4-chloroquinolin-3-amines and 4-chloro[1,5]naphthyridin-3-amines of Formula XX are known. Others can be prepared using conventional synthetic methods; for example, by reduction of known 4-chloro-3-nitroquinolines and 4-chloro-3-nitro[1,5]naphthyridines.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088788B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-d5a88e4ec13f445e8fe622339e34cee5 |
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| Source note | uspto-grants-2012_01 |
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