Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(3-Chloropyrazin-2-YL)morpholine | HCID 20528994 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 86681229 | HCID 86681229 | 92.9% |
Reaction Steps
A mixture of 4-(3-chloropyrazin-2-yl)morpholine (894 mg, 6 mmol) and aq NaOH (13 mL, 52 mmol) in DMSO (18 mL) was stirred at 80° C. for 2 h. The reaction mixture was poured into water (30 mL) and extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give 3-morpholinopyrazin-2(1H)-one as a light yellow solid (807 mg, 92.9%). 1H NMR (300 MHz, CDCl3) δ 11.80 (br s, 1H), 7.05 (d, J=4.2 Hz, 1H), 6.73 (d, J=4.2 Hz, 1H), 3.84 (s, 8H). LCMS (ESI) m/z 182 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08952058B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-20f3fa5ed99a4bf289fd2bfc2bd56382 |
|---|
| Source note | uspto-grants-2015_02 |
|---|