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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712268Generated: October 29, 2026

Dimethylformamide → 1-(5-(Benzyloxy)-7-cyanobenzo[d]thiazol-2-yl)-3-ethylurea

https://huagongshe.com/reaction/712268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1-(5-Benzyloxy-7-bromo-benzothiazol-2-yl)-3-ethyl-ureaHCID 57813629—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystZinc AcetateHCID 11192—
CatalystZincHCID 23994—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Product1-(5-(Benzyloxy)-7-cyanobenzo[d]thiazol-2-yl)-3-ethylureaHCID 86663980100%

Reaction Conditions

Temperature100 °C

Reaction Steps

1-(5-(benzyloxy)-7-bromobenzo[d]thiazol-2-yl)-3-ethylurea (5.00 g, 12.29 mmol), zinc cyanide (1.58 g, 13.49 mmol), 1,1′-bis(diphenylphosphino)ferrocene (20 mg, 0.033 mmol), zinc acetate (90 mg, 0.50 mmol) and zinc dust (33.3 mg, 0.50 mmol) were stirred in a reaction tube in degassed DMF (60 ml) and water (600 ul). Tris(dibenzylideneacetone)dipalladium(0) (113.2 mg, 0.133 mmol) was added and the reaction purged with N2, sealed and heated to 100° C. for 18 h with stirring. LCMS indicated clean conversion to the desired material. The solvents were removed under reduced pressure, the resulting residue triturated with water, the solid collected by filtration and dried in a vacuum oven to afford the desired material as a pale white solid 4.4 g (100%). This material was used directly in the next step with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-c254583292a64119901cd80fe1599e1c
Source noteuspto-grants-2015_11