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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470506Generated: November 2, 2026

1-Hydroxybenzotriazole → 5-Chloroisoquinolin-4-carboxylic amide

https://huagongshe.com/reaction/1470506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-Chloroisoquinoline-4-carboxylic acidHCID 68281964—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-Chloroisoquinolin-4-carboxylic amideHCID 6828189370%

Reaction Steps

A 100 mL RBF was charged with 5-chloroisoquinolin-4-carboxylic acid (1 equiv) in dry THF (20 mL), DIPEA (3 equiv), EDC.HCl (1.5 equiv), HOBT (1.5 equiv) under inert atmosphere and the mixture was stirred for 15 mins. To this, corresponding amine (1.2 equiv) was added dropwise and the reaction mixture was stirred overnight. After completion, it was diluted with EtOAc and water. The organic layer was then separated, dried and concentrated under reduced pressure to give the crude product that was purified by column chromatography using 100-200 silica gel (80% Ethyl acetate in Hexanes) to furnish the desired amide derivative in 70-84% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006442B2
Source datasetuspto-grants-2015_04
ORD IDord-0f4b566d253a4322a9b310816c4f3244
Source noteuspto-grants-2015_04