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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555406Generated: October 27, 2026

Chlorosuccinimide → HCID 59857382, compound

https://huagongshe.com/reaction/555406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant2-(2-Tert-butylphenoxy)pyridin-3-amineHCID 28605427—
SolventDimethylformamideHCID 6228—
ProductHCID 59857382HCID 5985738268%

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of N-chlorosuccinimide (556 mg, 4.2 mmol) in DMF (10 ml) was added to a solution of 1b (960 mg, 4.0 mmol) in DMF (15 ml) at rt. The reaction was heated at 40° C. for 30 min. The reaction mixture was cooled to rt and the reaction was quenched with saturated aqueous sodium thiosulfate (Na2S2O3) solution (100 mL). The mixture was extracted with ethyl acetate (3×20 ml) and the organic layers were washed with aqueous sodium thiosulfate solution, brine and were dried over sodium sulfate. The solvents were removed under reduced pressure and the dark red oil was purified by chromatography on silica (continuous gradient 0 to 40% Hexane/EtOAc) to give 125a as an off-white solid (746 mg, 68% yield). [M+H]+=277.11. 1H NMR (500 MHz, CDCl3): 7.41 (d, 1H, J=7.4 Hz), 7.20 (t 1H, J=7.4 Hz), 7.11 (t, 1H, J=7.4 Hz), 7.01 (d, 1H, J=8.1 Hz), 6.93 (d, 1H, J=8.1 Hz), 6.85 (d, 1H, J=8.1 Hz), 3.91 (s, 1H), 1.39 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053450B2
Source datasetuspto-grants-2011_11
ORD IDord-ce4159f343824ee292969289e0490d05
Source noteuspto-grants-2011_11