HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029493Generated: October 26, 2026
Water → 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-oxo-1-isoindolinyl 2-methylpropoxyacetate
https://huagongshe.com/reaction/1029493
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutoxyacetyl chloride | HCID 14146847 | — |
| Reactant | 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-hydroxy-1-isoindolinone | HCID 14182181 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-oxo-1-isoindolinyl 2-methylpropoxyacetate | HCID 70056296 | 62.6% |
Reaction Steps
To a solution, maintained at a temperature in the region of 20° C., of 2-(7-methoxy-1,8-naphthyridin-2-yl)-3-hydroxy-1-isoindolinone (9.2 g) and triethylamine (20 cc) in 1,2-dichloroethane (150 cc), there is added, in the course of 20 minutes, a solution of 2-methylpropoxyacetyl chloride (9 g) in 1,2-dichloroethane (20 cc) followed by 4-dimethylaminopyridine (50 mg), and the mixture is heated to reflux for 16 hours. The reaction mixture is poured into water (250 cc) and then extracted with methylene chloride (100 cc.) After the extract is washed with water, dried and concentrated to dryness under reduced pressure (3kPa), the residue obtained is purified by two successive recrystallizations in ethanol. 2-(7-Methoxy-1,8-naphthyridin-2-yl)-3-oxo-1-isoindolinyl 2-methylpropoxyacetate (7.9 g), m.p. 114° C., is thereby obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102890 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-4e787b3984744ff483c373a4c8c3e2d9 |
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| Source note | uspto-grants-1992_04 |
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