Pyrrolidine → HCID 12493615, compound
Reaction equation
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.Cl[N:7]1[CH:12]=[C:11]([Cl:13])[CH2:10][N:9](Cl)[NH:8]1>>[Cl:13][C:11]1[C:12]([N:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)=[N:7][N:8]=[N:9][C:10]=1[N:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1Participants
3
Procedure
Pyrrolidine (28.5 g) is cooled on an ice bath. 1,3,5-Trichlorotriazine (18.4 g) is added with vigorous stirring. After 1-1.5 h the mixture is permitted to warm to 20°-25°. The solid is filtered and rinsed several times with water and dried under reduced pressure to give the monochloro-bis(1-pyrrolidinyl)triazine.
Workup
- temperatureto warm to 20°-25°
- filtrationThe solid is filtered
- washrinsed several times with water
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-d1b3a901513942fcb4e874959a2de6c8
- Source dataset
- uspto-grants-1993_12
- Patent number
- US05268477
Reaction notes
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