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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2077515Generated: October 26, 2026

Acetic Anhydride → N-(7-bromobenzo[d]thiazol-2-yl)acetamide

https://huagongshe.com/reaction/2077515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Benzothiazolamine, 6-bromo-HCID 85149—
ReactantN-(6-bromo-1,3-benzothiazol-2-yl)acetamideHCID 3240669—
Reactant7-Bromo-1,3-benzothiazol-2-amineHCID 20357112—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(7-bromobenzo[d]thiazol-2-yl)acetamideHCID 5758491472%

Reaction Steps

The mixture (1.02 g, 4.45 mmol) of 7-bromobenzo[d]thiazol-2-amine and 6-bromobenzo[d]thiazol-2-amine and DMAP (620.6 mg, 5.079 mmol) were suspended in DCM (40 mL) and acetic anhydride (0.46 mL, 4.9 mmol) was added. The reaction was stirred under nitrogen at RT for 2 hours and was then quenched with 1 N HCl (25 mL). The layers were separated, and the aqueous phase was extracted with DCM, and the organic extracts were washed with 1 N HCl, dried over sodium sulfate, filtered, and concentrated to provide the mixture (865 mg, 72% yield) of N-(7-bromobenzo[d]thiazol-2-yl)acetamide and N-(6-bromobenzo[d]thiazol-2-yl)acetamide. MS (ESI pos. ion) m/z: 271 (MH+, 79Br), 273 (MH+, 81Br). Calculated exact mass for C9H7BrN2S: 270 (79Br), 272 (81Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928140B2
Source datasetuspto-grants-2011_04
ORD IDord-676de2c98c8446698854ab6e1ba52e74
Source noteuspto-grants-2011_04