4-(2-Chloroethyl)morpholine → HCID 20467857, compound

HRID 1903046Notes

Reaction equation

HRID 1903046 reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH:10]1[C:15]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:14]([CH3:21])[NH:13][N:12]=[C:11]1[C:22]([O:24][CH2:25][CH3:26])=[O:23])([O-:3])=[O:2].Cl[CH2:28][CH2:29][N:30]1[CH2:35][CH2:34][O:33][CH2:32][CH2:31]1>>[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH:10]1[C:15]([C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:14]([CH3:21])[N:13]([CH2:28][CH2:29][N:30]2[CH2:35][CH2:34][O:33][CH2:32][CH2:31]2)[N:12]=[C:11]1[C:22]([O:24][CH2:25][CH3:26])=[O:23])([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 767274-(2-Chloroethyl)morpholineHCID 20467859HCID 20467859, compound

Product 1

HCID 20467857HCID 20467857, compound

Procedure

This compound is prepared using the procedure of Example 1 from diethyl 1,4-dihydro-4-(2-nitrophenyl)-6-methyl-3,5-pyridazine dicarboxylate and N-(2-chloroethyl)morpholine.

Workup

  1. customThis compound is prepared

Sources & evidence

ORD record
ord-31c564acffe9483ebf8e2dde2ef77a39
Source dataset
uspto-grants-1984_03
Patent number
US04435395

Reaction notes

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