Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 86665107 | HCID 86665107 | — |
| Product | HCID 67130014 | HCID 67130014 | 20% |
Reaction Steps
A flask was charged with N4-cyclopropyl-N2-(4-fluoro-3-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-6-yl)furo[3,2-d]pyrimidine-2,4-diamine (0.19 g, 0.45 mmol, prepared using B from Preparation #A.1 with Preparation #AN.1) and 4 M HCl in 1,4-dioxane (2 mL). The mixture was stirred at about 50° C. for about 2 h, cooled to rt, concentrated under reduced pressure and purified by reverse phase HPLC (Table 2, Method o) to give N4-cyclopropyl-N2-(4-methyl-1H-indazol-6-yl)furo[3,2-d]pyrimidine-2,4-diamine (0.030, 20%): LC/MS (Table 2, Method h) Rt=1.85 min; MS m/z: 321 (M+H)+. Syk IC50=A
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08551981B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-d486badac6d6486a964ae4581913a371 |
|---|
| Source note | uspto-grants-2013_10 |
|---|