HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555406Generated: October 27, 2026
Chlorosuccinimide → HCID 59857382, compound
https://huagongshe.com/reaction/555406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 2-(2-Tert-butylphenoxy)pyridin-3-amine | HCID 28605427 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59857382 | HCID 59857382 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08053450B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-ce4159f343824ee292969289e0490d05 |
|---|
| Source note | uspto-grants-2011_11 |
|---|