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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771396Generated: November 3, 2026

p-Toluenesulfonic acid → Methyl 5-((4-((4-aminonaphthalen-1-yl)oxy)pyrimidin-2-yl)amino)-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/1771396

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantDimethylformamideHCID 6228—
ReactantMethyl 5-amino-1H-indazole-3-carboxylateHCID 28819013—
ProductMethyl 5-((4-((4-aminonaphthalen-1-yl)oxy)pyrimidin-2-yl)amino)-1H-indazole-3-carboxylateHCID 90004981—

Reaction Steps

A solution of Intermediate E2 (1.60 g, 5.90 mmol), methyl 5-amino-1H-indazole-3-carboxylate (1.35 g, 7.07 mmol) and p-TSA (2.24 g, 11.8 mmol) in DMF (30 mL) was stirred at 60° C. for 16 hr. The reaction mixture was cooled to RT and was partitioned between EtOAc (100 mL) and saturated aq. NaHCO3 (100 mL). The layers were separated and the organic extract was washed with water (2×100 mL) and brine (2×100 mL) and then dried and evaporated in vacuo. The residue was purified by trituration with acetonitrile to afford the title compound Intermediate B16 as a brown solid (0.937 g, 87% pure by HPLC, 33%); Rt 1.67 min (Method 2, acidic); m/z 427 (M+H)+ (ES+). The material was used in subsequent steps without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249125B2
Source datasetuspto-grants-2016_02
ORD IDord-70320be93f9443b7853cf3306d487f4a
Source noteuspto-grants-2016_02