HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204480Generated: October 31, 2026
Ethyl Acetate → 1-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)ethanol
https://huagongshe.com/reaction/2204480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehyde | HCID 58009883 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)ethanol | HCID 58010200 | 23% |
Reaction Steps
To a solution of methylmagnesium chloride (0.232 mL, 0.697 mmol) in THF (10 mL) at about −78° C. was added a solution of 5-tosyl-5H-pyrrolo[2,3-b]pyrazine-2-carbaldehyde (0.210 g, 0.697 mmol, Example #10, Step B) in DCM (10.0 mL). After about 10 min saturated aqueous NH4Cl was added to the reaction mixture. After warming to room temperature, EtOAc (30 mL) was added to the reaction mixture and the organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 20-80% EtOAc/heptane to provide 1-(5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-yl)ethanol (0.050 g, 23%) as a yellow oil. LC/MS (Table 2, Method a) Rt=2.04 min; MS m/z: 318 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09365579B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-c85c60a22d764796851d294ce2b69573 |
|---|
| Source note | uspto-grants-2016_06 |
|---|