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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099761Generated: November 3, 2026

N-Methyl dicyclohexylamine → 7-Methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazole-5-carbaldehyde

https://huagongshe.com/reaction/2099761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl dicyclohexylamineHCID 24210—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant7-Methyl-1H-indazole-5-carbaldehydeHCID 18452106—
SolventTetrahydrofuranHCID 8028—
Product7-Methyl-2-((2-(trimethylsilyl)ethoxy)methyl)-2H-indazole-5-carbaldehydeHCID 11572862—

Reaction Steps

To a solution of 7-methyl-1H-indazole-5-carbaldehyde (5.0 g, 31.25 mmol) and N-methyl-dicyclohexylamine (13.5 mL, 62.35 mmol) in dry tetrahydrofuran (120 mL) at 0° C., was added 2-(trimethylsilyl)ethoxymethyl chloride (6.65 mL, 39.5 mmol). The ice-bath was removed and stirring continued for 5 h. The reaction mixture was diluted with ethyl acetate, washed with water (2×), brine (2×), dried over sodium sulfate, and concentrated in vacuo. Column chromatography afforded 8.5 g (93%). 1H-NMR (400 MHz, CDCl3) δ 12.3 (br., 1H), 8.13 (s, 1H), 7.88 (s, 1H), 7.42 (s, 1H), 6.12 (d, J=7.0 Hz, 1H), 5.31 (d, J=7.0 Hz, 1H), 3.80 (s, 3H), 2.60 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569578B2
Source datasetuspto-grants-2009_08
ORD IDord-e51fff9dd3a447aab3d5e42afa9dbb91
Source noteuspto-grants-2009_08