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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029509Generated: October 26, 2026

5-Methylhexanoyl chloride → 2-(7-Methyl-1,8-naphthyridin-2-yl)-3-oxo-1-isoindolinyl 5-methylhexanoate

https://huagongshe.com/reaction/1029509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methylhexanoyl chlorideHCID 13664865—
Reactant2-(7-Methyl-1,8-naphthyridin-2-yl)-3-hydroxy-1-isoindolinoneHCID 19900439—
SolventTriethylamineHCID 8471—
Product2-(7-Methyl-1,8-naphthyridin-2-yl)-3-oxo-1-isoindolinyl 5-methylhexanoateHCID 7005715674.2%

Reaction Steps

The procedure is as in example 7, but starting with 2-(7-methyl-1,8-naphthyridin-2-yl)-3-hydroxy-1-isoindolinone (3.7 g), 5-methylhexanoyl chloride (7.8 g), triethylamine (12 cc) and 4-diemthylaminopyridine (50 mg). After the solid obtained after treatment has been recrystallized in methylcyclohexane, 2-(7-methyl-1,8-naphthyridin-2-yl)-3-oxo-1-isoindolinyl 5-methylhexanoate (3.8 g), m.p. 144° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102890
Source datasetuspto-grants-1992_04
ORD IDord-1c52e89755fa4372a03b57242696e688
Source noteuspto-grants-1992_04