HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44124Generated: October 26, 2026
Water → N-(1H-benzimidazol-2-yl)-1,3-benzothiazol-2-amine
https://huagongshe.com/reaction/44124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2-Diaminobenzene (D4, 98%) | HCID 10772950 | — |
| Reactant | HCID 178504144 | HCID 178504144 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(1H-benzimidazol-2-yl)-1,3-benzothiazol-2-amine | HCID 15578107 | 60.1% |
Reaction Steps
O-phenylenediamine (21.6 g (0.2 mol)) was dissolved in 944 g of DMF, and thereto was added dropwise a solution obtained by dissolving 50.9 g (0.20 mol) of S,S′-dimethyl-N-(2-benzothiazolyl)-carbonimidodithioate in 1258 g of DMF. The resulting mixture was then heated to 153° C., refluxed under a nitrogen atmosphere for 13 hours, and then cooled to 0° C. Thereto was added dropwise 2000 g of water, and a precipitate was filtered off, washed with water, and dried to obtain 32.0 g of 2-(2-benzothiazolylamino)benzoimidazole (L8: see Table 1 below). The yield was 60.1% based on o-phenylenediamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08540904B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-fac1acc8c38b43438104ddd3a7536cf4 |
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| Source note | uspto-grants-2013_09 |
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