Reacción #632014

Ecuación de reacción

1-methoxymethylcyclopropylsulfonylamine tert-butyl-carbamate

n-propyl isocyanate

→

1-propylcarbamoylcyclopropanesulfonamide tert-butylcarbamate

Rendimiento 100.0%

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThis compound was obtained in a crude 100% yield
2. 2
   OtroThe compound was taken directly into the next reaction without purification

Procedimiento

This compound was obtained in a crude 100% yield according to the procedure described for the synthesis of 1-methoxymethylcyclopropylsulfonylamine tert-butyl-carbamate using 1.10 equivalents of n-propyl isocyanate as the electrophile. The compound was taken directly into the next reaction without purification: 1H NMR (CDCl3) δ 0.10 (m, 2H), 0.51 (m, 2H), 0.67 (m, 1H), 1.10 (m, 2H), 1.49 (s, 9H), 1.62 (m, 2H), 1.87 (d, J=7.0 Hz, 2H).

Fuente