HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 15147492, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 15147488 | HCID 15147488 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15147492 | HCID 15147492 | — |
Reaction Steps
A mixture of 5-tert-butyloxycarbonylamino-6-methyl-2-phenyl-4-(4-pyridyl)pyrimidine (1.5 g) and an isopropanol solution of hydrogen chloride (4 ml, HCl 5 mMol/ml) in ethanol (15 ml) was stirred for 1 hour at 40° C. After cooling to room temperature, the reaction mixture was poured into a suspension of ethyl acetate (100 ml) and water (50 ml) under stirring, and the mixture was adjusted to pH 9.0. The separated organic layer was washed with saturated aqueous sodium chloride and dried over magnesium sulfate. The solvent was evaporated in vacuo, and the residual crystal was recrystallized from ether to give 5-amino-6-methyl-2-phenyl-4-(4-pyridyl)pyrimidine, mp 208°-209° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04698340 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-7ee07a3da02a4973b97531e0c6f2cfd9 |
| Source note | uspto-grants-1987_10 |