HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429863Generated: October 29, 2026
Benzo(d)thiazol-2-amine → HCID 9932706, compound
https://huagongshe.com/reaction/429863
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzo(d)thiazol-2-amine | HCID 8706 | — |
| Reactant | HCID 22335512 | HCID 22335512 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 9932706 | HCID 9932706 | 9% |
Reaction Steps
A mixture of 1-[2-ethyl-1-(4-isothiocyanatophenyl)butyl]-1H-imidazole (0.0123 mol) and 2-benzothiazolamine (0.0148 mol) in acetonitrile (80 ml) was stirred and refluxed for 12 hours. The solvent was evaporated and the residue was taken up in H2O and CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97.5/2.5/0.1). The desired fractions were collected and the solvent was evaporated. The residue was purified again by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 85/15/0.1). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from 2-butanone and DIPE. The precipitate was filtered off and dried, yielding 0.44 g (9%) (±)-N-(2-benzothiazolyl)-N′-[4-[1-(1H-imidazol-1-yl)-2-ethylbutyl]phenyl]-thiourea (compound 705).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06319939B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-4d4477b8540a4cf290ef8ee22c106931 |
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| Source note | uspto-grants-2001_11 |
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