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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595791Generated: October 31, 2026

1H-Indazol-6-amine → 4-(1H-indazol-6-ylamino)-7-methoxy-quinoline-3-carbonitrile

https://huagongshe.com/reaction/1595791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indazol-6-amineHCID 81423—
ReactantPyridinium chlorideHCID 10176127—
Reactant4-Chloro-7-methoxyquinoline-3-carbonitrileHCID 12559431—
SolventGlycol monoethyl etherHCID 8076—
Product4-(1H-indazol-6-ylamino)-7-methoxy-quinoline-3-carbonitrileHCID 996666297.3%

Reaction Steps

Using an analogous procedure to that described in Example 141, 200.0 mg (0.914 mmol) of 4-chloro-7-methoxy-3-quinolinecarbonitrile in 10 mL of 2-ethoxyethanol and in the presence of 105.6 mg (0.914 mmol) of pyridine hydrochloride was reacted with 147.8 mg (1.1 mmol) of 6-aminoindazole to give 280.0 mg (97.3%) of the product as a deep yellow solid, m.p.>250° C., mass (electrospray, m/e): M+H 315.9. HRCIMS: calcd 315.112 for C18H13N5O (M+), obsd 315.1124.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288082B1
Source datasetuspto-grants-2001_09
ORD IDord-5ca7f6bbe11c46e7b2d9b1aa2a51ca11
Source noteuspto-grants-2001_09