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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055548Generated: November 1, 2026

Diisopropylethylamine → HCID 59657535, compound

https://huagongshe.com/reaction/2055548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant3H-spiro[2-benzofuran-1,4'-piperidine]HCID 10442498—
Reactant6-Chloro-2-methyl-1H-indole-3-carboxylic acidHCID 45121065—
SolventDimethylformamideHCID 6228—
ProductHCID 59657535HCID 5965753549.7%

Reaction Steps

To a solution of 0.040 g (0.19 mmol) 6-chloro-2-methyl-1H-indole-3-carboxylic acid, 0.069 ml (0.40 mmol) N,N-diisopropylethylamine and 0.061 g (0.19 mmol) 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate in 1 ml dry N,N-dimethylformamide were added 0.036 g (0.19 mmol) spiro[isobenzofuran-1(3H), 4′-piperidine] at room temperature. After stirring for 1 h the reaction mixture was quenched with 0.5 M aqueous sodium hydroxide solution (20 ml) and extracted with ethyl acetate (2×30 ml). The combined organic layers were washed with water (2×30 ml) and brine (1×30 ml), dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography (n-heptane/ethyl acetate) to give the title compound (0.036 g, 49%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332501B2
Source datasetuspto-grants-2008_02
ORD IDord-6525a800472c43e096e2ab6479552074
Source noteuspto-grants-2008_02