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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240241Generated: October 30, 2026

2-Chloro-4-nitroaniline → HCID 59304984, compound

https://huagongshe.com/reaction/2240241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-nitroanilineHCID 8492—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant4-Chloro-1H-pyrrolo[2,3-b]pyridineHCID 11389493—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solventtert-ButanolHCID 6386—
ProductHCID 59304984HCID 59304984—

Reaction Conditions

Temperature100 °C

Reaction Steps

Variant B: A mixture of 200 mg (1.31 mmol) of 4-chloro-1H-pyrrolo[2,3-b]pyridine, 678 mg (3.93 mmol) of 2-chloro-4-nitroaniline, 60 mg (0.07 mmol) of tris(dibenzylideneacetone)dipalladium, 62 mg (0.13 mmol) of dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine and 399 mg (2.88 mmol) of potassium carbonate and 2.50 ml of degassed tert-butanol is stirred in a sealed pressure vessel at 100° C. for 3 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723347B2
Source datasetuspto-grants-2010_05
ORD IDord-f42f7cfcb8d047c5b303fb7e3b54a553
Source noteuspto-grants-2010_05