Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 59333702 | HCID 59333702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59333763 | HCID 59333763 | — |
Reaction Steps
(S)-tert-Butyl 2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-4-((tetrahydrofuran-2-yl)methylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (75 mg, 0.15 mmol) was dissolved in methanol (3 mL). Hydrochloric acid (4.51 μL, 0.15 mmol) was added and the reaction mixture was stirred at 75° C. for 1 h. The solvent was evaporated under reduced pressure and the crude (S)-N2-(4-(2-methyl-1H-imidazol-1-yl)phenyl)-N4-((tetrahydrofuran-2-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4-diamine (55.0 mg, 91%) was used as such in the subsequent step. MS (ES+) m/z 406.3 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08188101B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-dbae75497f75462c8b39d94ce4fee3ec |
|---|
| Source note | uspto-grants-2012_05 |
|---|