HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → ethyl 4-(3-(2-(aminomethyl)acrylamido)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | ethyl 4-(3-(2-((tert-butoxycarbonylamino)methyl) acrylamido)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate | HCID 89630003 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | ethyl 4-(3-(2-(aminomethyl)acrylamido)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate | HCID 89630004 | — |
Reaction Steps
A solution of ethyl 4-(3-(2-((tert-butoxycarbonylamino)methyl) acrylamido)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate (50 mg, 0.11 mmol) in 4 M HCl in dioxane solution (537 μL, 2.15 mmol) was stirred for 1 hour. The reaction mixture was quenched with aqueous saturated sodium bicarbonate (500 μL) and extracted with ethyl acetate (×3). The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by chromatography on silica eluting with 0-20% MeOH/DCM to give ethyl 4-(3-(2-(aminomethyl)acrylamido)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate. LRMS (ESI) calc'd for C19H20N5O3 [M+H]+: 366, found 366.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08993756B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-5e19673c2688472bae15413192bdf2d1 |
| Source note | uspto-grants-2015_03 |