Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 89629948 | HCID 89629948 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 89629949 | HCID 89629949 | — |
Reaction Steps
To a solution of ethyl 4-(2-methyl-2H-indazol-6-yl)-7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate in MeOH (2.0 mL) was added 2 M aqueous LiOH (1.1 mL) and the reaction mixture was heated at 60° C. for 17 hours. The reaction mixture was then acidified with AcOH and extracted with EtOAc (×3). The combined organic layers were then washed with brine, dried with sodium sulfate, filtered and concentrated under reduced pressure to give 4-(2-methyl-2H-indazol-6-yl)-7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylic acid. No further purification was carried out. LRMS (ESI) calc'd for C21H26SiN5O3 [M+H]+: 424, found 424.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08993756B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-f8fbd37936bc4f3da70d18eae53fc037 |
|---|
| Source note | uspto-grants-2015_03 |
|---|