Methylamine → HCID 20392501, compound
Reaction equation
Cl.C([O:5][C:6]1[C:7]([CH3:23])=[N:8][C:9]([CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:10]([CH2:14]Cl)[C:11]=1[CH2:12]Cl)(=O)C.[CH3:24][NH2:25]>CS(C)=O>[CH3:24][N:25]1[CH2:12][C:11]2[C:6]([OH:5])=[C:7]([CH3:23])[N:8]=[C:9]([CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:10]=2[CH2:14]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
A mixture of 37.5 g (100 millimoles) of 2-methyl-4,5-di-(chloromethyl)-6-benzyl-pyridin-3-yl acetate hydrochloride (Example 4), 50 ml of dry dimethylsulfoxide and 16 g (500 millimoles) of methylamine is heated for 5 hours at 80° C. in an autoclave. The solvent is stripped off in a high vacuum and the residue is partitioned between methylene chloride and water, taking care that the pH of the aqueous phase is 7.
Workup
- customthe residue is partitioned between methylene chloride and water
Sources & evidence
- ORD record
- ord-e6fd9f05dbce4339ad5fb680d9578d06
- Source dataset
- uspto-grants-1979_09
- Patent number
- US04168379
Reaction notes
Loading…