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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882141Generated: November 3, 2026

1,4-Dioxane → ethyl 4-(3-(2-(aminomethyl)acrylamido)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

https://huagongshe.com/reaction/882141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactantethyl 4-(3-(2-((tert-butoxycarbonylamino)methyl) acrylamido)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylateHCID 89630003—
SolventHydrochloric AcidHCID 313—
Productethyl 4-(3-(2-(aminomethyl)acrylamido)phenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993756B2
Source datasetuspto-grants-2015_03
ORD IDord-5e19673c2688472bae15413192bdf2d1
Source noteuspto-grants-2015_03