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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237287Generated: October 31, 2026

N,N-Dimethyl-1,3-propanediamine → HCID 131727218, compound

https://huagongshe.com/reaction/2237287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
ReactantCesium carbonateHCID 10796—
Reactant2,2,6,6-Tetramethyl-3,5-heptanedioneHCID 70700—
ReactantHCID 59852933HCID 59852933—
CatalystCuprous chlorideHCID 62652—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 131727218HCID 1317272187.7%

Reaction Conditions

Temperature120 °C

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 CuCl (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714138B2
Source datasetuspto-grants-2010_05
ORD IDord-0ff5b9ccc06a49799ed3e4287b937c26
Source noteuspto-grants-2010_05