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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9133Generated: October 27, 2026

1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylurea → 1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/reaction/9133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-Phenylacetylenyl-2-benzothiazolyl)-3-ethylureaHCID 21985545—
CatalystLindlars catalystHCID 131709914—
SolventEthanolHCID 702—
Product1-(6-(2(Z)-Phenylvinyl)-2-benzothiazolyl)-3-ethylureaHCID 8658897341%

Reaction Steps

A suspension of 1-(6-phenylacetylenyl-2-benzothiazolyl)-3-ethylurea (0.032 g, 83% purity by weight, 0.083 mmol) and Lindlar catalyst (0.030 g, 5% weight purity, 0.012 mmol, 0.15 eq) in 2 mL ethanol was purged with nitrogen gas, followed by bubbling of hydrogen gas. It was stirred under hydrogen atmosphere for about 36 hours. The mixture was taken up in 10 mL MeOH, filtered, concentrated, and purified by preparative TLC to give 0.011 g (41%) of the desired compound. LC/MS 324 (M+1); LC retention time 2.84 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091227B2
Source datasetuspto-grants-2006_08
ORD IDord-b034843c1eae49b58ee346d1b1960c87
Source noteuspto-grants-2006_08