Bambuterol hydrochloride
Bambuterol hydrochloride Basic information
- Product Name:
- Bambuterol hydrochloride
- Synonyms:
-
- KWD-2183
- BAMBUTEROL HCL
- BAMBUTEROL HYDROCHLORIDE
- BAMBEC
- Bambuterol monohydrochloride
- dimethylcarbamic acid 5-[2[(1,1-dimethyl)amino]1-hydroxyethyl]-1,3-phenylene ester hydrochloride
- DIMETHYLCARBAMIC ACID 5-[2-[(1,1-DIMETHYLETHYL)AMINO]-1-HYDROXYETHYL]-1,3-PHENYLENE ESTER HYDROCHLORIDE
- Bambuterol hydrochloride, 98%, a long acting beta-adrenoceptor agonist (LABA)
- CAS:
- 81732-46-9
- MF:
- C18H30ClN3O5
- MW:
- 403.9
- EINECS:
- 643-060-9
- Product Categories:
-
- BAMBEC
- Bambuterol
- Amines
- Aromatics
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Active Pharmaceutical Ingredients
- Mol File:
- 81732-46-9.mol
Bambuterol hydrochloride Chemical Properties
- Melting point:
- 222-224°C
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- H2O: ~33 mg/mL, soluble
- form
- powder
- color
- off-white
- Merck
- 14,953
- InChIKey
- LBARATORRVNNQM-UHFFFAOYSA-N
- CAS DataBase Reference
- 81732-46-9(CAS DataBase Reference)
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
- HS Code
- 29242990
MSDS
- Language:English Provider:SigmaAldrich
Bambuterol hydrochloride Usage And Synthesis
Description
Bambuterol is an inactive prodrug of terbutaline. It has a prolonged duration of action when administered orally.
Chemical Properties
White Solid
Uses
Ester prodrug of the ?-adrenergic agonist terbutaline
Uses
Ester prodrug of the ?2-adrenergic agonist terbutaline.
Uses
beta adrenergic agonist, bronchodilator, cholinesterase inhibitor
Definition
ChEBI: The hydrochloride salt of bambuterol. A long acting beta-adrenoceptor agonist used in the treatment of asthma, it is a prodrug for terbutaline.
Synthesis
Conventionally, as a method for preparing bambuterol hydrochloride, bis-3,5- (N, N-dimethylcarba) is subjected to an acylation process from 3 ′, 5′-dihydroxyacetophenone represented by the following reaction formula in US Pat. No. 4419364. Preparing moyloxy) -acetophenone (step 1); Preparing a bis-3 ′, 5 ′-(N, N-dimethylcarbamoyloxy) -2-bromo-acetophenone therefrom (step 2); Preparing an bis-3 ′, 5 ′-(N, N-dimethylcarbamoyloxy) -2- (N-benzyl tert-butyl) amino-acetophenone from the alkylation process therefrom (step 3); From this step to prepare a 1- [bis- (3 ', 5'-N, N-dimethylcarbamoyloxy) phenyl] -2-N-3 tert-butylaminoethanol hydrochloride, ie bambuterol hydrochloride.
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