Benzaldehyde → HCID 178521796, compound

HRID 2284119Notes

Reaction equation

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

Participants

Reactant 2

HCID 240Benzaldehyde

HCID 86673961HCID 86673961, compound

Product 1

HCID 178521796HCID 178521796, compound

Procedure

Compound 204 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(1,2,3,4-tetrahydronaphthalen-2-oyl)aniline and benzaldehyde. [M+H]+ calcd for C24H21N3O: 368.17; found: 368.00.

Sources & evidence

ORD record: ord-96594e62a853424196f6e0c54265bc3a
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

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