Ethylamine → HCID 18630106, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Si:8]([CH3:11])([CH3:10])[CH3:9])[C:3]=1[N:12]=[C:13]=[O:14].[CH2:15]([NH2:17])[CH3:16].C(OCC)(=O)C>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Si:8]([CH3:10])([CH3:11])[CH3:9])[C:3]=1[NH:12][C:13]([NH:17][CH2:15][CH3:16])=[O:14]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of the compound of Example h (4 mmol) in 50 mL toluene was added 70% ethyl amine (4 mL). The solution was stirred for 0.5 h and then stood overnight. Ethyl acetate was added and the mixture was washed with water. The organic layer was concentrated to a semisolid, which was triturated with hexane. The title compound was collected by filtration as 0.9 g of crystals, an 83% yield. m.p. 161-163° C.
Workup
- waitstood overnight
- washthe mixture was washed with water
- concentrationThe organic layer was concentrated to a semisolid, which
- customwas triturated with hexane
- filtrationThe title compound was collected by filtration as 0.9 g of crystals
Sources & evidence
- ORD record
- ord-67ba3f7e6f3c441c890bc507a24717e4
- Source dataset
- uspto-grants-2000_02
- Patent number
- US06028101
Reaction notes
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