Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661341Generated: November 2, 2026

Nitrogen → HCID 13837878, compound

https://huagongshe.com/reaction/661341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTetrahydrofuranHCID 8028—
ReactantOxindoleHCID 321710—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ProductHCID 13837878HCID 1383787857%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of oxindole 9 (6.25 g, 47 mmol) in THF (500 ml) was cooled to −78° C. and to it a solution of sodium hexamethyldisilazide (43 g, 235 mmol) in THF (300 ml) was added drop wise under N2 atmosphere. After stirring at −78° C. for 45 min, N-methylbis(2-chloromethyl)amine hydrochloride (9 g, 47 mmol) was added, as a solid. The reaction mixture was stirred at −78° C. for 1 h and at room temperature for 24 h. After quenching with H2O (90 ml), the mixture was extracted with ethyl acetate (3×100 ml). The organic extracts were washed with brine (25 ml), dried and the solvent removed in vacuo. Silica gel chromatography (5-50% MeOH/CH2Cl2, gradient) gave 6 g (57%) of 10 as a solid. 1HNMR (CD3OD, 400 MHz) δ 1.84 (m, 2H); 2.51 (m, 2H); 2.62 (s, 3H); 3.02 (m, 2H); 3.37 (m, 2H); 6.82 (d, 1H, J=7.68 Hz); 6.94 (t, 1H, J=7.58 Hz); 7.12 (t, 1H, J=7.7 Hz); 7.26 (d, 1H, J=9 Hz); 9.27 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084609B2
Source datasetuspto-grants-2011_12
ORD IDord-adf16c1c8d114034bda07aa9a3ef725f
Source noteuspto-grants-2011_12