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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099830Generated: October 25, 2026

N-Methyl dicyclohexylamine → 4-tert-Butyl 1-methyl 2-((7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)methyl)succinate

https://huagongshe.com/reaction/2099830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl dicyclohexylamineHCID 24210—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant4-Tert-Butyl 1-methyl 2-((7-methyl-1H-indazol-5-yl)methyl)succinateHCID 57794720—
SolventTetrahydrofuranHCID 8028—
Product4-tert-Butyl 1-methyl 2-((7-methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazol-5-yl)methyl)succinateHCID 69072989—

Reaction Steps

To a solution of 4-tert-butyl 1-methyl 2-((7-methyl-1H-indazol-5-yl)methyl)succinate (0.6053 g, 1.82 mmol) and N-cyclohexyl-N-methylcyclohexanamine (0.4686 mL, 2.19 mmol) in tetrahydrofuran (10 mL) was added trimethylsilylethoxymethyl chloride (0.3859 mL, 2.19 mmol) at room temperature under nitrogen. The reaction was stirred overnight and the solvent was removed in vacuo. The crude product was taken up in ethyl acetate (10 mL) and washed with water (3×5 mL). The ethyl acetate layer was dried, filtered and concentrated. The final product was obtained by flash chromatography, eluting with 0% to 20% ethyl acetate/hexane. (0.5873 g, 70%) HPLC tR=1.89 min, MS(ESI)[M+H]+=462.94.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569578B2
Source datasetuspto-grants-2009_08
ORD IDord-0ef70621c5d8428ba9a0501e688a9681
Source noteuspto-grants-2009_08