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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278837Generated: October 26, 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/2278837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmbroxolHCID 2132—
ReactantAcefyllineHCID 69550—
SolventTolueneHCID 1140—
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

The mixture of ambroxol base (378.1 g, 1 mole) and toluene (3000 ml) was heated at 60-65° C. for 1-2 minutes to prepare a clear solution. Toluene (1900 ml) and theophylline-7-acetic acid (238.2 g, 1 mole) were charged in a round bottom flask and heated at 75 to 80° C. To this flask, the prepared solution of ambroxol base in toluene was added under stirring while maintaining the temperature between 75-80° C. during 2-3 minutes. The resulting reaction mixture was stirred at 100-105° C. for 25-30 minutes. The reaction mixture was allowed to cool to room temperature. The separated solid product was filtered and washed with toluene and dried. The yield of Acebrophylline obtained was 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133196B2
Source datasetuspto-grants-2015_09
ORD IDord-df1417d907a34af5bb9b200241ea25f1
Source noteuspto-grants-2015_09