HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → (3-Bromo-8-morpholinoimidazo[1,2-b]pyridazin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (8-Morpholinoimidazo[1,2-b]pyridazin-2-yl)methanol | HCID 117728752 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (3-Bromo-8-morpholinoimidazo[1,2-b]pyridazin-2-yl)methanol | HCID 117728706 | — |
Reaction Steps
A solution of compound 5d (40.0 g, 171 mmol) in CH3CN (400 mL) was treated dropwise with a solution of NBS (30.2 g, 170 mmol) in CH3CN (906 mL) at −20° C. After addition, the reaction mixture was stirred for 2 h at room temperature. The reaction was quenched by the addition of 50 mL of saturated Na2S2O3 solution. The solids formed were collected by filtration and washed with diethyl ether to afford compound 83a as a white solid. Mass Spectrum (LCMS, ESI pos.): Calcd. for C11H13BrN4O2: 313.0 (M+H). found: 313.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193736B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-cff34138d71540a6ac2d3c1c8da7bb51 |
| Source note | uspto-grants-2015_11 |