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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181443Generated: November 3, 2026

Sodium Azide → HCID 85869868, compound

https://huagongshe.com/reaction/1181443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantOxalyl chlorideHCID 65578—
ReactantIsoquinoline-5-carboxylic acid monohydrateHCID 69523124—
CatalystDimethylformamideHCID 6228—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 85869868HCID 8586986844%

Reaction Steps

Isoquinoline-5-carboxylic acid monohydrate (5.00 g, 26.2 mmol) was suspended in dichloromethane (200 ml) and N,N-dimethylformamide (5 drops) added. Oxalyl chloride (4.57 ml, 52 mmol) was then added and the reaction stirred for 7 h. The solvent and excess oxalyl chloride was then evaporated and the residue taken up in dichloromethane (200 ml). A solution of sodium azide (2.1 g, 32.3 mmol) and tetra-n-butylammonium bromide (850 mg) in water (50 ml) was then added in one portion and the mixture stirred for 20 min. The layers were separated and the aqueous phase extracted with more dichloromethane (100 ml). The combined organic phases were evaporated and the residue purified by flash column chromatography (eluant ethyl acetate-dichloromethane (1:4)) to give the title compound as a yellow solid (2.27 g, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285563B2
Source datasetuspto-grants-2007_10
ORD IDord-9baf64d6536d4ab58a56d81ff92ab0a5
Source noteuspto-grants-2007_10