5-(Morpholin-4-yl)thiophene-2-carboxaldehyde → HCID 178521813, compound

HRID 2284209Notes

Reaction equation

HRID 2284209 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:22]=[CH:23][C:24]=1[N+:25]([O-])=O)[NH:7][C:8](=[O:21])[C:9]1[CH:14]=[CH:13][C:12]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][CH2:16]2)=[CH:11][CH:10]=1)([O-])=O.[O:28]1[CH2:33][CH2:32][N:31]([C:34]2[S:38][C:37]([CH:39]=O)=[CH:36][CH:35]=2)[CH2:30][CH2:29]1>>[O:28]1[CH2:33][CH2:32][N:31]([C:34]2[S:38][C:37]([C:39]3[NH:25][C:24]4[CH:23]=[CH:22][C:6]([NH:7][C:8](=[O:21])[C:9]5[CH:14]=[CH:13][C:12]([N:15]6[CH2:20][CH2:19][O:18][CH2:17][CH2:16]6)=[CH:11][CH:10]=5)=[CH:5][C:4]=4[N:1]=3)=[CH:36][CH:35]=2)[CH2:30][CH2:29]1

Participants

3

Procedure

Compound 418 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-morpholinobenzoyl)aniline and 5-morpholinothiophene-2-carboxaldehyde. [M+H]+ calcd for C26H27N5O3S: 490.18; found: 489.95.

Sources & evidence

ORD record
ord-52e68d7792db4c3a9a54b905ade454d7
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

Loading…