HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374067Generated: October 30, 2026
N,N-Dimethyl-1,3-propanediamine → HCID 131727218, compound
https://huagongshe.com/reaction/2374067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2,2,6,6-Tetramethyl-3,5-heptanedione | HCID 70700 | — |
| Reactant | HCID 59852933 | HCID 59852933 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 131727218 | HCID 131727218 | 7.7% |
Reaction Steps
A mixture of N-(4-(2-chloropyridin-4-yloxy)-3-fluorophenyl)-2,6-difluorobenzamide (70 mg, 0.19 mmol), 3-(dimethylamino)propylamine (44 mL, 0.35 mmol), Cs2CO3 (85 mg, 0.26 mmol) and CuCi (17 mg, 0.17 mmol) in a screw capped vial was purged with N2. NMP and 2,2,6,6,-tetramethyl-3,5-heptanedione (31 mg, 0.17 mmol) were added to the mixture which was then heated at 120° C. for 4 h. The mixture was cooled, partitioned between EtOAc and saturated aq. NaHCO3 solution and the EtOAc phase was separated, dried (MgSO4) and concentrated in vacuo to give the crude product. Purification of the residue by preparative HPLC (Column C) and conversion to the hydrochloride salt was carried out in a similar manner as Step D of Example 33 to give the title compound (7 mg, 7%) as an off-white solid. MS(ESI+): m/z 517.37 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07459562B2 |
|---|
| Source dataset | uspto-grants-2008_12 |
|---|
| ORD ID | ord-b6142dbbec61429a9a6b16147c6dcc11 |
|---|
| Source note | uspto-grants-2008_12 |
|---|