Reacción #586133

ord-e7876ddf05454d08b61143f95df42d8c

Ecuación de reacción

N#Cc1ccc(-c2ccc(Cl)s2)cc1F
4-(5-chlorothiophen-2-yl)-2-fluorobenzonitrile
Br.N=C(N)SCC1CC1
S-cyclopropylmethylisothiourea hydrobromide
N#Cc1ccc(-c2ccc(Cl)s2)cc1SCC1CC1
4-(5-chlorothiophen-2-yl)-2-cyclopropylmethylthiobenzonitrile
Rendimiento 91.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto react in the same manner

Procedimiento

0.9 g (4.0 mmol) of 4-(5-chlorothiophen-2-yl)-2-fluorobenzonitrile and 0.9 g (4.3 mmol) of S-cyclopropylmethylisothiourea hydrobromide were allowed to react in the same manner as described above in Example 8 (4), and purification of the crude product by silica gel column chromatography afforded 1.1 g of 4-(5-chlorothiophen-2-yl)-2-cyclopropylmethylthiobenzonitrile (yield 91%) as yellow feathery crystals (m.p. 123-124° C.).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07767626B2uspto-grants-2010_08