HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine → HCID 178468834, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Ethyl 4-[2-(5-amino-4-cyanofuran-3-yl)ethyl]benzoate | HCID 10826899 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178468834 | HCID 178468834 | — |
Reaction Steps
To a solution of guanidine free base (prepared from 105 mg of guanidine hydrochloride and 60 mg of sodium ethoxide) in 10 mL of anhydrous ethanol are added 284 mg (1 mmol) of ethyl 4-[2-(2-amino-3-cyanofur-4-yl)ethyl]benzoate. The mixture is heated at reflux for 30 hrs and the solvent then evaporated in vacuo. The residue is chromatographed on silica gel, eluting with 5:95 methanol:methylene chloride, to yield ethyl 4-{2-(2,4-diaminopyrrolo[2,3-d]pyrimidin-5-yl)ethyl}benzoate as a light brown solid; m.p. 202°-204° C. Mass spectrograph calculated for C17H19N5O2 : 325.1538, Found: 325.1543.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254687 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-72a670814b5243518c237d3feb9e283a |
| Source note | uspto-grants-1993_10 |