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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615356Generated: October 30, 2026

2-BENZOTHIAZOLESULFONAMIDE, 6-NITRO- → Aminozolamide

https://huagongshe.com/reaction/615356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BENZOTHIAZOLESULFONAMIDE, 6-NITRO-HCID 13393427—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductAminozolamideHCID 9350526.2%

Reaction Steps

6-Nitro-2-benzothiazolesulfonamide (2.93 g., 0.0113 mole) suspended in absolute ethanol (200 ml.) was hydrogenated in the presence of 5% palladium on carbon (2.9 g.) in a Parr apparatus. After 5 hrs. the reaction mixture was filtered to remove the catalyst, and the filtrate was concentrated to dryness to give the solid product. Recrystallization from ethyl acetate and reprecipitation by dissolution in dilute aqueous hydrochloric acid followed by treatment with aqueous sodium bicarbonate solution gave 680 mg 6-amino-2-benzothiazolesulfonamide, m.p. 227°-9° C. dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04499103
Source datasetuspto-grants-1985_02
ORD IDord-c653603eed5a4b27a3d8e85a5be552b0
Source noteuspto-grants-1985_02