Reaktion #9218

ord-9a4c0e1c1fc94c6586402782e0c32725

Reaktionsgleichung

[Li][CH2]CCC
n-BuLi
CCNC(=O)Nc1nc2ccc(Br)c(OC(C)C)c2s1
1-(6-bromo-7-isopropoxy-2-benzothiazolyl)-3-ethylurea
O=C1CCC(=O)N1Cl
N-chlorosuccinimide
CCNC(=O)Nc1nc2cccc(OC(C)C)c2s1
title compound
Ausbeute 25.1%
CCNC(=O)Nc1nc2cccc(OC(C)C)c2s1
1-(7-Isopropoxy-2-benzothiazolyl)-3-ethylurea
Ausbeute 25.1%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigepurified by HPLC

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091227B2uspto-grants-2006_08