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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014469Generated: October 30, 2026

Hydrochloric Acid → HCID 59442045, compound

https://huagongshe.com/reaction/1014469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 59441716HCID 59441716—
Reactant2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-6-fluorobenzamideHCID 86644188—
Solvent2,2,2-TrifluoroethanolHCID 6409—
SolventSodium BicarbonateHCID 516892—
ProductHCID 59442045HCID 59442045—

Reaction Steps

A mixture of 5-(methyloxy)-1-[(4-methylphenyl)sulfonyl]-2,3-dihydro-1H-indol-6-amine (4.0 g, 12.5 mmol), 2-({2-chloro-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)-6-fluorobenzamide (8.6 g, 18.79 mmol) and a 4 N solution of HCl in dioxane (16 mL, 62.5 mmol) in 2,2,2-trifluoroethanol (250 mL) was heated overnight in a sealed vessel at 80° C. The reaction mixture was diluted with a saturated NaHCO3 solution, and the resulting slurry was filtered and the solids were taken up into THF (1L). The resulting slurry was filtered and the filtrate was concentrated. The resulting orange solid was dissolved in THF (250 mL), and a 27% aqueous NH4OH solution (250 mL) was added and the reaction mixture was stirred overnight. The organic volatiles were evaporated, and the residue was extracted with CH2Cl2 (3×200 mL). The organic layers were combined, dried (Na2SO4), concentrated onto Celite and purified by silica gel chromatography using 0-2%THF/CH2Cl2 to obtain 2-fluoro-6-({2-({5-(methyloxy)-1-[(4-methylphenyl)sulfonyl]-2,3-dihydro-1H-indol-6-yl}amino)-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)benzamide as a yellow solid (2.8 g, 30% for 2 steps). ESIMS (M+H)+=742.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-8133f0a5b74c4fb0a5f754e0ef8251d0
Source noteuspto-grants-2011_07