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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908671Generated: October 30, 2026

Triethylamine → 5-[(3-Bromopropyl)amino]-2-methyl-1,3-benzothiazole-4,7-dione

https://huagongshe.com/reaction/908671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Bromopropylamine hydrobromideHCID 78701—
Reactant5-Methoxy-2-methylbenzo[d]thiazole-4,7-dioneHCID 481756—
SolventMethanolHCID 887—
Product5-[(3-Bromopropyl)amino]-2-methyl-1,3-benzothiazole-4,7-dioneHCID 67393455—

Reaction Conditions

Temperature60 °C

Reaction Steps

1.57 g (7.17 mmol; 1.5 equivalent) of 3-bromopropylamine hydrobromide and 1.02 ml (7.17 mmol; 1.5 equivalent) of triethylamine are added to 1 g (4.78 mmol) of 5-methoxy-2-methyl-1,3-benzothiazole-4,7-dione in solution in 100 ml of methanol. The reaction mixture is maintained under stirring for 2 hours at 60° C., then the solvent is evaporated off under reduced pressure and the residue is purified by chromatography on a silica column (eluent: dichloromethane/methanol: 97/3). The 5-[(3-bromopropyl)amino]-2-methyl-1,3-benzothiazole-4,7-dione is obtained in the form of a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017637B2
Source datasetuspto-grants-2011_09
ORD IDord-b9043b773b5c4588894fef0a83f1752a
Source noteuspto-grants-2011_09