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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278836Generated: October 25, 2026

Ambroxol → (1,3-Dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-7H-purin-7-yl)acetic acid--4-(((2-amino-3,5-dibromophenyl)methyl)amino)cyclohexan-1-ol (1/1)

https://huagongshe.com/reaction/2278836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmbroxolHCID 2132—
ReactantAcefyllineHCID 69550—
SolventChloroformHCID 6212—
Product(1,3-Dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-7H-purin-7-yl)acetic acid--4-(((2-amino-3,5-dibromophenyl)methyl)amino)cyclohexan-1-ol (1/1)HCID 176595—

Reaction Conditions

Temperature62.5 °C

Reaction Steps

Ambroxol base (20.0 g, 0.052 moles) was dissolved in chloroform (100 ml) at room temperature. Chloroform (100 ml) and theophylline-7-acetic acid (12.6 g, 0.052 moles) were charged in a round bottom flask and heated at 60 to 65° C. To this flask, the prepared solution of ambroxol base in chloroform was added under stirring while maintaining the temperature between 60-65° C. during 2-3 minutes. The resulting reaction mixture was stirred at 60-65° C. for 25-30 minutes. The reaction mixture was allowed to cool to room temperature. The separated solid product was filtered and washed with chloroform and dried. The yield of Acebrophylline obtained was 97.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133196B2
Source datasetuspto-grants-2015_09
ORD IDord-de2d709f7c914403ac17e3f500fa2ebb
Source noteuspto-grants-2015_09