HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531284Generated: October 31, 2026
1,1'-Carbonyldiimidazole → HCID 72188769, compound
https://huagongshe.com/reaction/531284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 4-{5-[4-({(4S,5R)-5-[3,5-Bis(trifluoromethyl)phenyl]-4-methyl-2-oxo-1,3-oxazolidin-3-yl}methyl)-2-(3-fluoroazetidin-1-yl)pyrimidin-5-yl]-6-methoxypyridin-3-yl}-3,5-dimethylbenzohydrazide | HCID 90009093 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 72188769 | HCID 72188769 | — |
Reaction Steps
A solution of 4-{5-[4-({(4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-4-methyl-2-oxo-1,3-oxazolidin-3-yl}methyl)-2-(3-fluoroazetidin-1-yl)pyrimidin-5-yl]-6-methoxypyridin-3-yl}-3,5-dimethylbenzohydrazide (Step A, 90 mg, 0.120 mmol) in THF (1.2 mL) was treated with N,N-carbonyldiimidazole (58.6 mg, 0.361 mmol). The reaction was stirred at room temperature overnight. The reaction was purified directly by silica gel chromatography, eluting with a gradient of 25-100% ethyl acetate/hexanes to give the titled compound. LCMS (M+H)+: 774.6. 1H NMR (CDCl3, 500 MHz): δ 9.12 (br, 1H), 8.17 (s, 1H), 8.03 (d, 1H), 7.89 (s, 1H), 7.74 (s, 2H), 7.61 (d, 2H), 7.31 (d, 1H), 5.71 (d, 1H), 5.51 (m, 0.5H), 5.40 (m, 0.5H), 4.71 (d, 1H), 4.47 (m, 3H), 4.31 (m, 2H), 4.01 (m, s, 4H), 2.16 (s, 3H), 2.15 (s, 3H), 0.76 (d, 3H). RTA IC50: 8 nM
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09353101B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-05e0167921514900aa64a52231679063 |
|---|
| Source note | uspto-grants-2016_05 |
|---|