Morpholine → HCID 13175260, compound
Reaction equation
Cl[C:2]1[CH:14]=[CH:13][C:5]2=[N:6][C:7]3[CH2:12][CH2:11][CH2:10][CH2:9][C:8]=3[N:4]2[N:3]=1.[NH:15]1[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1>>[N:15]1([C:2]2[CH:14]=[CH:13][C:5]3=[N:6][C:7]4[CH2:12][CH2:11][CH2:10][CH2:9][C:8]=4[N:4]3[N:3]=2)[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1Participants
3
Procedure
A mixture was prepared by adding 5.0 g of 2-chloro-6,7,8,9-tetrahydropyridazino[1,6-a]benzimidazole to 30 ml of morpholine and this was stirred and heated at reflux for 24 hours. It was then poured into 200 ml of ice water. A tan solid formed and this was separated by filtration to give 2-(4-morpholinyl)-6,7,8,9-tetrahydropyridazino[1,6-a]benzimidazole melting at 187.5°-188.5° C.
Workup
- customA mixture was prepared
- temperatureheated
- temperatureat reflux for 24 hours
- customA tan solid formed
- customthis was separated by filtration
Sources & evidence
- ORD record
- ord-dc5e57af1b4a498394618e559a8fb055
- Source dataset
- uspto-grants-1983_07
- Patent number
- US04391806
Reaction notes
Loading…