Ethyl 3-oxohexanoate → HCID 178439481, compound

HRID 489377Notes

Reaction equation

HRID 489377 reaction equation
[CH2:1]1[C:9]2[CH:8]=[CH:7][CH:6]=[C:5]([CH:10]=O)[C:4]=2[CH2:3][CH2:2]1.[NH2:12][C:13]1[CH:17]=[CH:16][NH:15][N:14]=1.O=[C:19]([CH2:26][CH2:27][CH3:28])[CH2:20][C:21]([O:23][CH2:24][CH3:25])=[O:22]>>[CH2:1]1[C:9]2[C:4](=[C:5]([CH:10]3[C:20]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:19]([CH2:26][CH2:27][CH3:28])[NH:12][C:13]4=[N:14][NH:15][CH:16]=[C:17]34)[CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1

Participants

4

Reactant 3

HCID 238498Ethyl 3-oxohexanoateHCID 5761352,3-dihydro-1H-indene-4-carbaldehydeHCID 178418806HCID 178418806, compound

Product 1

HCID 178439481HCID 178439481, compound

Procedure

The title compound was prepared from indan-4-aldehyde, 3-aminopyrazole and ethyl 3-ketohexanoate in the same manner as in Example 1.

Sources & evidence

ORD record
ord-54aec4185db540079b8a01cf06c9f5fc
Source dataset
uspto-grants-2005_12
Patent number
US06977262B2

Reaction notes

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