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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052114Generated: November 1, 2026

(5-Benzyloxy-3-cyano-indazol-1-yl)-acetic acid tert-butyl ester → Tert-butyl 2-(3-cyano-5-(pyrimidin-2-ylmethoxy)-1H-indazol-1-yl)acetate

https://huagongshe.com/reaction/1052114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Benzyloxy-3-cyano-indazol-1-yl)-acetic acid tert-butyl esterHCID 90020069—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 2-(3-cyano-5-(pyrimidin-2-ylmethoxy)-1H-indazol-1-yl)acetateHCID 90020049—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of (5-benzyloxy-3-cyano-indazol-1-yl)-acetic acid tert-butyl ester (4 g, 11.01 mmol) in THF (400 mL) was added Pd/Al2O3 (5%) (4.10 g, 38.5 mmol). The reaction mixture was stirred at 40° C. for 16 h under H2 atmosphere (4 bars). The reaction mixture was filtered through a pad of Celite, which was then washed with CH2Cl2. The combined organics were concentrated under vacuum to give the title compound as a yellow solid. MS (LC/MS): 296.0 [M+Na]+; tR (conditions e): 4.46 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388199B2
Source datasetuspto-grants-2016_07
ORD IDord-4b10d92000f9498499590a821424a432
Source noteuspto-grants-2016_07