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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586444Generated: October 30, 2026

Benzo(d)thiazol-2-amine → HCID 9932706, compound

https://huagongshe.com/reaction/586444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(d)thiazol-2-amineHCID 8706—
ReactantHCID 22335512HCID 22335512—
SolventAcetonitrileHCID 6342—
ProductHCID 9932706HCID 99327069%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936626B2
Source datasetuspto-grants-2005_08
ORD IDord-ab8c2600263d4ffb8bf9c1cbaab04e07
Source noteuspto-grants-2005_08