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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661597Generated: October 29, 2026

Toluene → HCID 58215614, compound

https://huagongshe.com/reaction/1661597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantChloromethyl pivalateHCID 87885—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant2-pyridin-3-yl-1H-indole-5-carbonitrileHCID 44554135—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58215614HCID 58215614—

Reaction Steps

To a solution of 2-pyridin-3-yl-1H-indole-5-carbonitrile (Example 8, 210 mg, 1.37 mmol) in THF (20 mL) at room temperature is added 0.5 M KHMDS in toluene (4.1 mL, 2.05 mmol). After 30 min, chloromethyl pivalate (510 mg, 3.08 mmol) is added. The mixture is stirred under N2 for 1 h. Saturated aqueous sodium bicarbonate (0.5 mL) is added to quench the reaction. Silica gel is added to the mixture and the solvents are removed in vacuo. The residue is purified by silica gel flash chromatography (ethyl acetate-heptane, 0:1 to 1:0). Further purification by HPLC using an Xbridge RP18 with a gradient of 0.1% aqueous ammonium hydroxide in acetonitrile gives 2,2-dimethyl-propionic acid 5-cyano-2-pyridin-3-yl-indol-1-ylmethyl ester as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 1.20 (s, 9H), 6.08 (s, 2H), 6.77 (s, 1H), 7.49 (ddd, J=7.8, 4.8, 0.8 Hz, 1H), 7.56 (dd, J=8.6, 1.8 Hz, 1H), 7.68 (d, J=8.6 Hz, 1H), 7.94 (ddd, J=7.9, 2.0 Hz, 1H), 8.01 (dd, J=1.5, 0.5 Hz, 1H), 8.75 (dd, J=4.8, 1.8 Hz, 1H), 8.87 (d, J=1.5 Hz, 1H). HRMS (ESI) m/z 334.1566 [(M+H)+ Calcd for C20H20N3O2: 334.1556].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030334B2
Source datasetuspto-grants-2011_10
ORD IDord-c300ec4bf971408dba11725b209145be
Source noteuspto-grants-2011_10