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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435970Generated: October 31, 2026

Phthaloyl chloride → (S)-3-[1-(1,3-dioxo-1,3-dihydroisoindol-2-yl)isoquinolin-6-yloxy]piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1435970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthaloyl chlorideHCID 6955—
ReactantTriethylamineHCID 8471—
Reactant(S)-3-(1-amino-isoquinolin-6-yloxy)piperidin-1-carboxylic acid tert-butyl esterHCID 68875514—
SolventWaterHCID 962—
Product(S)-3-[1-(1,3-dioxo-1,3-dihydroisoindol-2-yl)isoquinolin-6-yloxy]piperidine-1-carboxylic acid tert-butyl esterHCID 6887439474.2%

Reaction Steps

To a solution of (S)-3-(1-amino-isoquinolin-6-yloxy)piperidin-1-carboxylic acid tert-butyl ester (380 mg, 1.11 mmol) and triethylamine (1.5 ml, 11.1 mmol) in anhydrous tetraydrofuran (1.5 ml) was added phthaloyl dichloride (170 μL, 1.16 mmol). The mixture was stirred at ambient temperature for 2 h and then poured into quickly stirring water. The mixture was extracted with dichloromethane (3×50 ml) and concentrated in vacuo to give a residue. Flash chromatography of the residue on silica (eluent: 0-100% ethyl acetate in heptane) gave (S)-3-[1-(1,3-dioxo-1,3-dihydroisoindol-2-yl)isoquinolin-6-yloxy]piperidine-1-carboxylic acid tert-butyl ester (390 mg) E1l-MS: m/z=474.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618985B2
Source datasetuspto-grants-2009_11
ORD IDord-4722e7cd784f4e37bac0dee730fa5e1d
Source noteuspto-grants-2009_11