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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946999Generated: November 4, 2026

HCID 59743357, compound → HCID 178472431, compound

https://huagongshe.com/reaction/1946999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59743357HCID 59743357—
ReactantHCID 178472434HCID 178472434—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178472431HCID 17847243133.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

1-(2-Methanesulfonylpyrimidin-4-yl)-1H-indazole (6.4 g) was suspended in THF and the mixture heated to 60° C. until complete dissolution of the solids. trans-4-Amino-cyclohexane-carboxylic acid ethyl ester (7.99 g, 46.6 mmol) was added, followed by TEA (9.7 mL, 69.9 mmol), and the resulting mixture stirred overnight. The reaction mixture was concentrated under reduced pressure until solids started to precipitate, and was then heated to 60° C. for 24 h. THF (4 mL) was added, and the reaction mixture stirred for 64 h at 60° C. The resulting mixture was extracted with EtOAc, the combined organic extracts washed with water, dried over MgSO4, filtered, and evaporated under reduced pressure. The crude residue was purified by flash chromatography (DCM/MeOH, 98:2) and the brown solid obtained was triturated with Et2O to give trans-4-(4-indazol-1-ylpyrimidin-2-ylamino)-cyclohexanecarboxylic acid ethyl ester (2.883 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399462B2
Source datasetuspto-grants-2013_03
ORD IDord-c7ece807f54746e4bb896f07308da206
Source noteuspto-grants-2013_03