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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108902Generated: October 29, 2026

(6-Nitro-benzothiazol-2-yl)-carbamic acid tert-butyl ester → HCID 58305681, compound

https://huagongshe.com/reaction/2108902

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Nitro-benzothiazol-2-yl)-carbamic acid tert-butyl esterHCID 58305710—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
ProductHCID 58305681HCID 5830568177.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

6-Nitrobenzothiazol-2-yl tert-butyl carbamate (4.68 g, 15.8 mmol) was dissolved in dimethylformamide (120 mL) and palladium on charcoal (841 mg, 10% Pd, 0.79 mmol Pd) was added. The air was replaced with hydrogen (1 bar) and the mixture was vigorously stirred at 60° C. until completion of the reaction (2 h). The palladium was removed by filtration through a pad of celite and the solution was concentrated to 20 mL. Water (200 mL) was added. After stirring for 1 h, the precipitated 6-aminobenzothiazol-2-yl tert-butyl carbamate was filtered off and washed with water. Additional product was obtained by repeated filtration of the mother liquor. A total of 3.24 g (12.2 mmol, 77%) of a grey solid was obtained. LC/ESI-MS: m/z=266 [M+H]+; m/z=264 [M−H]−; Rt=2.54 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514460B2
Source datasetuspto-grants-2009_04
ORD IDord-a062798eb91d47fa9bc4e1a335b686dd
Source noteuspto-grants-2009_04