Dimethyl malonate → HCID 66760244, compound

Reaction equation

[CH:1]1[C:13]2[NH:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][C:2]=1[C:14](=[O:23])[CH:15]=[CH:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.[C:24]([O:31][CH3:32])(=[O:30])[CH2:25][C:26]([O:28][CH3:29])=[O:27]>>[CH:1]1[C:13]2[NH:12][C:11]3[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=3)[C:5]=2[CH:4]=[CH:3][C:2]=1[C:14](=[O:23])[CH2:15][CH:16]([CH:25]([C:24]([O:31][CH3:32])=[O:30])[C:26]([O:28][CH3:29])=[O:27])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

Reactant 2

HCID 7943Dimethyl malonate

HCID 66759599HCID 66759599, compound

Product 1

HCID 66760244HCID 66760244, compound

Procedure

By a procedure similar to that of example 1.59.2, starting from 1-(9H-carbazol-2-yl)-3-phenylprop-2-en-1-one and dimethyl malonate, dimethyl 2-(3-(9H-carbazol-2-yl)-3-oxo-1-phenylpropyl)malonate was obtained as colourless solid.

Sources & evidence

ORD record: ord-d3fae2f03f72483596fa014a3df38b52
Source dataset: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08912186B2

Reaction notes

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