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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772348Generated: November 3, 2026

Tert-butyl 4-(4-chlorobenzoyl)-3-methylisothiazol-5-ylcarbamate → (5-Amino-3-methylisothiazol-4-yl)(4-chlorophenyl)methanone

https://huagongshe.com/reaction/1772348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-chlorobenzoyl)-3-methylisothiazol-5-ylcarbamateHCID 67814309—
SolventTrifluoroacetic acidHCID 6422—
Product(5-Amino-3-methylisothiazol-4-yl)(4-chlorophenyl)methanoneHCID 6781414074.8%

Reaction Steps

To tert-butyl 4-(4-chlorobenzoyl)-3-methylisothiazol-5-ylcarbamate (2.80 g, 7.94 mmol) was added an excess of TFA (20 mL). After a period of 15 min at reflux, the reaction mixture was evaporated under reduced pressure to give (5-amino-3-methylisothiazol-4-yl)(4-chlorophenyl)methanone as a white solid (1.50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249161B2
Source datasetuspto-grants-2016_02
ORD IDord-17cae3036e9141de9da3f527d97d94ad
Source noteuspto-grants-2016_02