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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423132Generated: October 31, 2026

Hydrochloric Acid → Ivabradine

https://huagongshe.com/reaction/423132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantBromocresol GreenHCID 6451—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(3-(((7S)-3,4-dimethoxy-7-bicyclo(4.2.0)octa-1,3,5-trienyl)methylamino)propyl)-7,8-dimethoxy-2,5-dihydro-1H-3-benzazepin-4-one;hydrochlorideHCID 66672699—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductIvabradineHCID 13299958%

Reaction Steps

180 mg (0.36 mmol) of hydrochloride obtained in Step 1 are dissolved in a mixture of 10 mL of methanol and 5 mL of dichloromethane. To the resulting solution there are added 0.04 mL (0.54 mmol, 1.5 equivalents) of formaldehyde (37% in water) and a grain of bromocresol green. 1N aqueous hydrochloric acid solution is added until the pH is 4 (yellow-coloured solution) and then stirring is carried out at 25° C. for 30 minutes. There are then added 23 mg (0.36 mmol) of sodium cyanoborohydride, stirring is carried out at 25° C. for 12 hours whilst maintaining the pH at 4, and then evaporation to dryness is carried out. There are obtained 250 mg of an oil which is purified by flash chromatography on 100 g of silica (eluant=dichloromethane/ethanol/NH4OH: 90/10/1) to yield 100 mg of the title product in the form of a colourless oil which crystallises at ambient temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101747B2
Source datasetuspto-grants-2012_01
ORD IDord-e802e191876048489e5ecf67bb84d89a
Source noteuspto-grants-2012_01