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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408617Generated: October 30, 2026

Indole → HCID 68176377, compound

https://huagongshe.com/reaction/408617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86702031HCID 86702031—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68176377HCID 68176377—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of indole (1 eq.) in THF is added NaH (1.5 eq., 60% in oil) and the mixture is stirred at 20° C. for 1 h. A solution of 4-[(4-Chloro-benzyl)-(1-chlorocarbonyl-2-methyl-azetidine-2-carbonyl)-amino]-butyric acid methyl ester in THF in added dropwise and the mixture is stirred at 20° C. for 16 h. The mixture was concentrated and the residue dissolved in EtOAc, washed with aqueous HCl (0.1N), a saturated aqueous solution of NaHCO3 and brine. The organic layer is dried over Na2SO4, filtered and concentrated under reduced pressure. The crude residue is used as such in next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-b60265b0d6754cedbd67f0f08a1ff394
Source noteuspto-grants-2014_06