Reacción #2383805

ord-fe43f75a723949d6b88c3bf6b625f220

Ecuación de reacción

NN.O
hydrazine hydrate
NN.O
hydrazine hydrate
O=c1[nH][nH]c(=O)c2c([N+](=O)[O-])cccc12
5-nitro-2,3-dihydrophthalazine-1,4-dione
O
water
Nc1cccc2c(=O)[nH][nH]c(=O)c12.[Na]
5-amino-2,3-dihydrophthalazine-1,4-dione sodium salt
Nc1cccc2c(=O)[nH][nH]c(=O)c12
5-amino-2,3-dihydrophthalazine-1,4-dione
NN.O
hydrazine hydrate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat 90-120° C.

Procedimiento

This problem was solved by a method for manufacturing 5-amino-2,3-dihydrophthalazine-1,4-dione sodium salt, comprising reduction of the product by hydrazine hydrate in presence of a skeletal nickel catalyst, first by interacting 3-nitro-phthalanhydride with hydrazine hydrate in acetic acid at 90-120° C. with formation of 5-nitro-2,3-dihydrophthalazine-1,4-dione, after reduction thereof by hydrazine hydrate in a water-alkaline medium in presence of a skeletal nickel catalyst, isolating 5-amino-2,3-dihydrophthalazine-1,4-dione, which is then treated by sodium hydroxide in the presence of a lower alcohol or a ketone at 20-80° C. to obtain the target product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06489326B1uspto-grants-2002_12