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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661664Generated: October 29, 2026

Potassium Phosphate, Tribasic → HCID 58215781, compound

https://huagongshe.com/reaction/1661664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant1-Boc-6-chloroindole-2-boronic acidHCID 44119151—
ReactantN-[(5-Bromo-3-pyridinyl)methyl]methanesulfonamideHCID 59534656—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 58215781HCID 58215781—

Reaction Conditions

Temperature85 °C

Reaction Steps

A flask is charged with N-(5-bromo-pyridin-3-ylmethyl)-methanesulfonamide (Example 163a, 530 mg, 2 mmol), N-Boc-6-chloro-indole-2-boronic acid (525 mg, 3.0 mmol), s-Phos (41 mg, 0.10 mmol), finely crushed potassium phosphate (849 mg, 4.0 mmol) and toluene (20 mL), and the mixture is degassed for 15 min. Pd2dba3 (37 mg, 0.04 mmol) is added and the mixture is stirred at 85° C. for 1 h. The mixture is cooled to room temperature, diluted with DCM and silica gel (10 g) is added. The mixture is concentrated in vacuo and the residue is purified by silica gel flash chromatography eluting with a 0 to 90% ethyl acetate-heptane gradient to give 6-chloro-2-[5-(methanesulfonylamino-methyl)-pyridin-3-yl]-indole-1-carboxylic acid tert-butyl ester. MS (ESI) m/z 436.1 and 437.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030334B2
Source datasetuspto-grants-2011_10
ORD IDord-99d478a4a07745b6a7f2634afb81995d
Source noteuspto-grants-2011_10