Technology Process of 2-(Tetrahydro-pyran-4-ylamino)-4-(1,5,5-trimethyl-7-oxo-4,5,6,7-tetrahydro-1H-indazol-3-yl)-benzonitrile
There total 9 articles about 2-(Tetrahydro-pyran-4-ylamino)-4-(1,5,5-trimethyl-7-oxo-4,5,6,7-tetrahydro-1H-indazol-3-yl)-benzonitrile which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
sodium t-butanolate;
tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;
In
toluene;
at 80 ℃;
for 4h;
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: sodium hydroxide; dihydrogen peroxide / methanol; water / -15 - 0 °C
2.1: methanol; potassium hydroxide / 20 °C / Heating / reflux
3.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.75 h / -20 - 20 °C
3.2: 1 h / -78 °C
4.1: acetic acid / methanol / 1.5 h / Heating / reflux
5.1: sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 4 h / 80 °C
With
methanol; potassium hydroxide; sodium hydroxide; dihydrogen peroxide; acetic acid; lithium hexamethyldisilazane; sodium t-butanolate;
tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;
In
tetrahydrofuran; methanol; water; toluene;
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: methanol; potassium hydroxide / 20 °C / Heating / reflux
2.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.75 h / -20 - 20 °C
2.2: 1 h / -78 °C
3.1: acetic acid / methanol / 1.5 h / Heating / reflux
4.1: sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 4 h / 80 °C
With
methanol; potassium hydroxide; acetic acid; lithium hexamethyldisilazane; sodium t-butanolate;
tris-(dibenzylideneacetone)dipalladium(0); 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl;
In
tetrahydrofuran; methanol; toluene;