4-Morpholinobenzaldehyde → HCID 178420603, compound

HRID 2284216Notes

Reaction equation

[N+:1]([C:4]1[CH:5]=[C:6]([C:13]2[O:14][C:15]([C:18]3[CH:23]=[CH:22][C:21]([N:24]4[CH2:29][CH2:28][O:27][CH2:26][CH2:25]4)=[CH:20][CH:19]=3)=[N:16][N:17]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[O:30]1[CH2:35][CH2:34][N:33]([C:36]2[CH:43]=[CH:42][C:39]([CH:40]=O)=[CH:38][CH:37]=2)[CH2:32][CH2:31]1>>[O:27]1[CH2:28][CH2:29][N:24]([C:21]2[CH:22]=[CH:23][C:18]([C:15]3[O:14][C:13]([C:6]4[CH:7]=[CH:8][C:9]5[NH:10][C:40]([C:39]6[CH:38]=[CH:37][C:36]([N:33]7[CH2:34][CH2:35][O:30][CH2:31][CH2:32]7)=[CH:43][CH:42]=6)=[N:1][C:4]=5[CH:5]=4)=[N:17][N:16]=3)=[CH:19][CH:20]=2)[CH2:25][CH2:26]1

Participants

Reactant 2

HCID 2913494-Morpholinobenzaldehyde

HCID 86673992HCID 86673992, compound

Product 1

HCID 178420603HCID 178420603, compound

Procedure

Compound 428 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-1-(5-(4-morpholinophenyl)-1,3,4-oxadiazol-2-yl)benzene and 4-morpholinobenzaldehyde. [M+H]+ calcd for C29H28N6O3: 590.23; found: 508.98.

Sources & evidence

ORD record: ord-c1cc76102a1943ccaac91b9b2594ec43
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

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