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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588149Generated: October 29, 2026

2-Methoxyaniline → 6-chloro-3-methoxy-N-(2-methoxyphenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-amine

https://huagongshe.com/reaction/588149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyanilineHCID 7000—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4,6-dichloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 118272510—
SolventTetrahydrofuranHCID 8028—
Product6-chloro-3-methoxy-N-(2-methoxyphenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-amineHCID 118272439—

Reaction Conditions

Temperature80 °C

Reaction Steps

4,6-dichloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridine (Intermediate 37B, 100 mg, 0.217 mmol), 2-methoxyaniline (26.0 μl, 0.217 mmol), t-butyl X-Phos palladacycle (5.97 mg, 8.69 μmol) were combined in a 5 ml microwave vial. The vial was evacuated and backfilled (3×) with N2 gas before adding THF (2.2 ml) and potassium t-butoxide (326 μl, 0.326 mmol). The reaction was allowed to stir at 80° C. for 2 hours. Room temperature was attained and the mixture was filtered through a celite frit and concentrated in vacuo while loading onto silica gel. Purifcation by MPLC 0-20% EtOAc/DCM gave 6-chloro-3-methoxy-N-(2-methoxyphenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-amine (52B). MS: [M+H]+ m/z 547.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226922B2
Source datasetuspto-grants-2016_01
ORD IDord-6329add573864d84849cbb603804ec8a
Source noteuspto-grants-2016_01