4-Nitrobenzoyl chloride → HCID 20226436, compound

HRID 1732028Notes

Reaction equation

HRID 1732028 reaction equation
[NH2:1][CH:2]1[CH2:6][N:5]([CH2:7][CH3:8])[N:4]([CH2:9][CH3:10])[CH2:3]1.[N+:11]([C:14]1[CH:22]=[CH:21][C:17]([C:18]([Cl:20])=[O:19])=[CH:16][CH:15]=1)([O-:13])=[O:12]>>[ClH:20].[N+:11]([C:14]1[CH:15]=[CH:16][C:17]([C:18]([NH:1][CH:2]2[CH2:6][N:5]([CH2:7][CH3:8])[N:4]([CH2:9][CH3:10])[CH2:3]2)=[O:19])=[CH:21][CH:22]=1)([O-:13])=[O:12]

Participants

3

Reactant 2

HCID 85024-Nitrobenzoyl chlorideHCID 5591991,2-Diethyl-4-pyrazolidinamine

Product 1

HCID 20226436HCID 20226436, compound

Procedure

The title compound was prepared as described in Example 4 of U.S. Pat. No. 4,207,327 from 4-amino-1,2-diethylpyrazolidine and p-nitrobenzoyl chloride.

Sources & evidence

ORD record
ord-2e813105dfd44bafa0e93b7402b584b7
Source dataset
uspto-grants-1986_11
Patent number
US04624961

Reaction notes

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