Diethyl (ethoxymethylene)malonate → HCID 178469654, compound
Reaction equation
[I:1][C:2]1[CH:8]=[C:7]([CH2:9][CH:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[CH:6]=[CH:5][C:3]=1[NH2:4].C([O:18][CH:19]=[C:20]([C:26](OCC)=O)[C:21]([O:23][CH2:24][CH3:25])=[O:22])C>C1(OC2C=CC=CC=2)C=CC=CC=1>[OH:18][C:19]1[C:5]2[C:3](=[C:2]([I:1])[CH:8]=[C:7]([CH2:9][CH:10]3[CH2:11][CH2:12][O:13][CH2:14][CH2:15]3)[CH:6]=2)[N:4]=[CH:26][C:20]=1[C:21]([O:23][CH2:24][CH3:25])=[O:22]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 130 °C
Procedure
A mixture of 2-iodo-4-(tetrahydro-2H-pyran-4-ylmethyl)aniline (1.0 g) and diethyl ethoxymethylenemalonate (0.70 mL) is heated at 130° C. for 1 h. The mixture is cooled to room temperature. Diphenyl ether (20 mL) is added and the reaction is heated to 250° C. for 1 h. The mixture is cooled and the resulting solid is collected and washed with hexanes. The crude product is chromatographed (Biotage flash 40M, eluent 2% MeOH/CH2Cl2) to yield 0.80 g (58%) of the desired product as an off-white solid.
Workup
- temperatureThe mixture is cooled to room temperature
- temperaturethe reaction is heated to 250° C. for 1 h
- temperatureThe mixture is cooled
- customthe resulting solid is collected
- washwashed with hexanes
- customThe crude product is chromatographed (Biotage flash 40M, eluent 2% MeOH/CH2Cl2)
Sources & evidence
- ORD record
- ord-2e566d8b55d44ae2981538f3009c8b76
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06727248B2
Reaction notes
Loading…