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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9152Generated: October 23, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → N-Ethyl-N'-[7-(3-pyridyl)[1,3]thiazolo[4',5': 3,4]benzo[d][1,3]thiazol-2-yl]urea

https://huagongshe.com/en/reaction/9152

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantN-Ethyl-N'-[7-(3-pyridyl)-4,5-dihydro[1,3]thiazolo[4',5': 3,4]benzo[d][1,3]thiazol-2-yl]ureaHCID 86588975—
SolventTolueneHCID 1140—
ProductN-Ethyl-N'-[7-(3-pyridyl)[1,3]thiazolo[4',5': 3,4]benzo[d][1,3]thiazol-2-yl]ureaHCID 992479730.1%

Reaction Conditions

Temperature35 °C

Reaction Steps

A suspension of N-ethyl-N′-[7-(3-pyridyl)-4,5-dihydro[1,3]thiazolo[4′,5′: 3,4]benzo[d]-[1,3]thiazol-2-yl]urea (10 mg, 0.028 mmol) and DDQ (13 mg, 0.056 mmol) in toluene (1 mL) was heated to about 35° C. for about 3 hrs. The reaction mixture was concentrated in vacuo and purified by preparative HPLC. 3 mg (30%) pure product was isolated. LC/MS 356 (MH+); RP-HPLC 14.25 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091227B2
Source datasetuspto-grants-2006_08
ORD IDord-990155086c5549828f0ac2fa7edc056a
Source noteuspto-grants-2006_08