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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9122Generated: October 25, 2026

Chlorosuccinimide → 1-(7-Isopropoxy-2-benzothiazolyl)-3-ethylurea

https://huagongshe.com/reaction/9122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant1-(6-Bromo-7-isopropoxy-2-benzothiazolyl)-3-ethylureaHCID 21985546—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1-(7-Isopropoxy-2-benzothiazolyl)-3-ethylureaHCID 2198565325.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1-(6-bromo-7-isopropoxy-2-benzothiazolyl)-3-ethylurea (0.036 g, 0.10 mmol) in 0.5 mL DME was cooled down to about −78° C., and was treated with a solution of 1.6 M n-BuLi in hexanes (0.16 mL, 0.26 mmol, 2.6 eq). It was stirred at the temperature for about 20 min, then a solution of N-chlorosuccinimide (NCS) (0.015 g, 0.11 mmol, 1.1 eq) in 0.5 mL DME was added. It was warmed up to about 0° C. for about 0.5 hour. It was taken up in MeOH and purified by HPLC to give 0.007 g (25%) of the title compound. LC/MS 279.9 (M+1); LC retention time 3.10 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091227B2
Source datasetuspto-grants-2006_08
ORD IDord-9a4c0e1c1fc94c6586402782e0c32725
Source noteuspto-grants-2006_08