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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529104Generated: October 31, 2026

Sodium bis(trimethylsilyl)amide → HCID 68737330, compound

https://huagongshe.com/reaction/529104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantN,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
ReactantHCID 22661266HCID 22661266—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68737330HCID 6873733042.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 2-oxoindoline-4-carbonitrile (2.97 g, 18.8 mmol; prepared as described in WO 00/21920) in THF (40 mL) was added dropwise a 1.0 M THF solution of NaHMDS (78.2 mL, 78.2 mmol) at about −78° C. under N2. After stirring at about −78° C. for about 30 min, N-benzylbis(2-chloroethyl)amine hydrochloride (4.20 g, 15.6 mmol) was added as a solid. The reaction mixture was stirred at about −78° C. for about 30 minutes and then allowed to warm to rt. The reaction mixture was then heated at reflux for 2 h. After cooling to about 0° C., the reaction was quenched by the addition of saturated aqueous NH4Cl solution. The reaction mixture was partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried and concentrated. The residue was purified by column chromatography (DCM:MeOH, 60:1) to give 1′-benzyl-2-oxospiro[indoline-3,4′-piperidine]-4-carbonitrile (2.10 g, 42%) as a solid. LCMS (APCI+) m/z 318 [M+H]+; Rt=2.42 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346805B2
Source datasetuspto-grants-2016_05
ORD IDord-247994519190458b8265c12e5a5722d6
Source noteuspto-grants-2016_05