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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | N,N-Bis(2-chloroethyl)benzylamine hydrochloride | HCID 2777881 | — |
| Reactant | HCID 22661266 | HCID 22661266 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68737330 | HCID 68737330 | 42.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346805B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-247994519190458b8265c12e5a5722d6 |
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| Source note | uspto-grants-2016_05 |
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