Methylamine → HCID 15053445, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][CH:15]=1)[O:5][CH:6]1[CH2:9][N:8]([C:10](Cl)=[O:11])[CH2:7]1.[CH3:16][NH2:17]>O1CCCC1.O>[Br:1][C:2]1[CH:3]=[C:4]([CH:13]=[CH:14][CH:15]=1)[O:5][CH:6]1[CH2:9][N:8]([C:10]([NH:17][CH3:16])=[O:11])[CH2:7]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A stirred solution of 5.8 g (0.02 mole) of 3-(3-bromophenoxy)-1 -azetidinecarbonyl chloride in 20 ml of tetrahydrofuran was treated with 4.7 g (0.06 mole) of 40 % aqueous monomethylamine. After stirring for 48 hr, the reaction mixture was diluted with 100 ml of water and the solid which formed was collected by filtration (6.0 g). Recrystallization from benzene yielded 2.0 g (35.1%) of tan crystals, m.p. 134°-135° C.
Workup
- customthe solid which formed
- filtrationwas collected by filtration (6.0 g)
- customRecrystallization from benzene
Sources & evidence
- ORD record
- ord-af591cc670fd4630b3e47726e6791669
- Source dataset
- uspto-grants-1991_11
- Patent number
- US05068231
Reaction notes
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