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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ambroxol | HCID 2132 | — |
| Reactant | Acefylline | HCID 69550 | — |
| Solvent | Chloroform | HCID 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09133196B2 |
|---|
| Source dataset | uspto-grants-2015_09 |
|---|
| ORD ID | ord-de2d709f7c914403ac17e3f500fa2ebb |
|---|
| Source note | uspto-grants-2015_09 |
|---|