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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromopropylamine hydrobromide | HCID 78701 | — |
| Reactant | 5-Methoxy-2-methylbenzo[d]thiazole-4,7-dione | HCID 481756 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-[(3-Bromopropyl)amino]-2-methyl-1,3-benzothiazole-4,7-dione | HCID 67393455 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017637B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-b9043b773b5c4588894fef0a83f1752a |
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| Source note | uspto-grants-2011_09 |
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