In the synthetic pathway, this compound undergoes cyclization with reagents such as formaldehyde or its derivatives to form the benzothiadiazine ring system, which is the core structure of hydrochlorothiazide. The presence of the amino, chloro, and sulfonamide groups in specific positions facilitates ring closure and subsequent functional group modifications, ultimately yielding the final thiazide diuretic with antihypertensive properties. 4-Amino-6-chloro-1,3-benzenedisulfonamide is a key intermediate in the synthesis of Hydrochlorothiazide.
4-Amino-6-chloro-1,3-benzenedisulfonamide
| API Name | Hydrochlorothiazide |
|---|---|
| CAS No | 121-30-2 |
| Molecular Formula | C6H8ClN3O4S2 |
| Molecular Weight | 285.7 g/mol |
| Synonyms | 4-amino-6-chlorobenzene-1,3-disulfonamide |
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Frequently Asked Questions
In the synthetic pathway, this compound undergoes cyclization with reagents such as formaldehyde or its derivatives to form the benzothiadiazine ring system, which is the core structure of hydrochlorothiazide. The presence of the amino, chloro, and sulfonamide groups in specific positions facilitates ring closure and subsequent functional group modifications, ultimately yielding the final thiazide diuretic with antihypertensive properties. 4-Amino-6-chloro-1,3-benzenedisulfonamide is a key intermediate in the synthesis of Hydrochlorothiazide.
The CAS number of 4-Amino-6-chloro-1,3-benzenedisulfonamide is 121-30-2.
The molecular formula of 4-Amino-6-chloro-1,3-benzenedisulfonamide is C6H8ClN3O4S2.
The listed molecular weight of 4-Amino-6-chloro-1,3-benzenedisulfonamide is 285.7 g/mol.
4-Amino-6-chloro-1,3-benzenedisulfonamide is listed as being used in connection with the following API: Hydrochlorothiazide.
The listed synonym or IUPAC name for 4-Amino-6-chloro-1,3-benzenedisulfonamide is 4-amino-6-chlorobenzene-1,3-disulfonamide.