Ethyl Acetoacetate → HCID 19808492, compound

HRID 373808Notes

Reaction equation

[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[CH2:2][C:3]([CH3:5])=[O:4].[C:10]1([N:20]2[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][Cl:28])[CH2:22][CH2:21]2)[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][CH:11]=1>>[ClH:28].[C:3]([CH:2]([CH2:27][CH2:26][N:23]1[CH2:24][CH2:25][N:20]([C:10]2[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[CH:13]=[CH:12][CH:11]=2)[CH2:21][CH2:22]1)[C:1]([O:7][CH2:8][CH3:9])=[O:6])(=[O:4])[CH3:5]

Participants

Reactant 2

HCID 8868Ethyl Acetoacetate

HCID 4741864HCID 4741864, compound

Product 1

HCID 19808492HCID 19808492, compound

Procedure

This compound was prepared according to the process described in Example 10, Stage C, from ethyl acetoacetate and 1-(1-naphthyl)-4-(2-chloroethyl)-piperazine.

Workup

customThis compound was prepared

Sources & evidence

ORD record: ord-04079ae549644b43a546b180c58ef553
Source dataset: uspto-grants-1992_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05166157

Reaction notes

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