Reacción #10896

ord-e2adeb5088e848eab7be6471672b965b

Ecuación de reacción

N#CN
cyanamide
CN1CCN(c2ccc(N=C=S)cc2)CC1
1-(4-isothiocyanatophenyl)-4-methylpiperazine
O=C(CBr)c1ccc2c(c1)OCO2
1-(1,3-benzodioxol-5-yl)-2-bromoethanone
O=C(CBr)c1ccc2c(c1)OCO2
1-(1,3-Benzodioxol-5-yl)-2-bromoethanone
CN1CCN(c2ccc(Nc3nc(N)c(C(=O)c4ccc5c(c4)OCO5)s3)cc2)CC1
[4-Amino-2-[[4-(4-methyl-1-piperazi nyl)phenyl]amino]-5-thiazolyl](1,3-benzodioxol-5-yl)methanone
Rendimiento 75.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

This compound was prepared in 75% yield from cyanamide (Aldrich), 1-(4-isothiocyanatophenyl)-4-methylpiperazine (of Example 1), and 1-(1,3-benzodioxol-5-yl)-2-bromoethanone (of Example 11) following the procedure used to in Example 24.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07094896B2uspto-grants-2006_08