HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216803Generated: October 26, 2026
Ethyl Acetate → 2-(1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/216803
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Reactant | 2-(1-(2,5-Dichloroquinolin-3-yl)ethyl)isoindoline-1,3-dione | HCID 57707873 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(1-(5-Chloro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)isoindoline-1,3-dione | HCID 57707828 | — |
Reaction Steps
Transferred 2-(1-(2,5-dichloroquinolin-3-yl)ethyl)isoindoline-1,3-dione (197 mg, 531 μmol) from 100 mL flask to 10 mL flask by dissolving/slurrying in toluene and concentrating. Added Pd(Ph3P)4 (61 mg, 53 μmol) and 2-tri-n-butylstannylpyridine (955 μl, 2653 μmol). Bubbled argon through mixture for 30 sec. Equipped with condenser and nitrogen inlet. Heated at 110° C. for ˜16 h. The reaction mixture was concentrated and chromatographed on 12 g silica gel column with 0-60% EtOAc. The desired fractions were combined and concentrated to yield an oil. NMR indicates residual EtOAc. LC. 1H NMR (400 MHz, DICHLOROMETHANE-d2) δ ppm 1.98 (d, J=7.04 Hz, 3H) 6.38 (q, J=7.04 Hz, 1H) 7.24-7.37 (m, 1H) 7.62-7.76 (m, 8H) 8.01 (dd, J=8.61, 1.96 Hz, 1H) 8.56-8.66 (m, 1H) 9.02 (s, 1H). −MS (+esi, M+H+=414.1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193199B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-a8ca35bace9a46e48d81d55ac316d421 |
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| Source note | uspto-grants-2012_06 |
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