HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278834Generated: 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/2278834
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ambroxol | HCID 2132 | — |
| Reactant | Acefylline | HCID 69550 | — |
| Solvent | Toluene | HCID 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 Steps
The mixture of ambroxol base (20.0 g, 0.052 moles) and toluene (160 ml) was heated at 60-65° C. for 1-2 minutes to prepare a clear solution. Toluene (100 ml) and theophylline-7-acetic acid (12.6 g, 0.052 moles) 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 98.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133196B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ae4d0d225ca6449c9837deafd3ff2a3d |
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| Source note | uspto-grants-2015_09 |
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