5-(4-Hydroxypiperidin-1-yl)thiophene-2-carboxaldehyde → HCID 178521805, compound

HRID 2284208Notes

Reaction equation

HRID 2284208 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.[OH:28][CH:29]1[CH2:34][CH2:33][N:32]([C:35]2[S:39][C:38]([CH:40]=O)=[CH:37][CH:36]=2)[CH2:31][CH2:30]1>>[OH:28][CH:29]1[CH2:34][CH2:33][N:32]([C:35]2[S:39][C:38]([C:40]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:37][CH:36]=2)[CH2:31][CH2:30]1

Participants

3

Procedure

Compound 417 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-morpholinobenzoyl)aniline and 5-(4-hydroxypiperidinyl)thiophene-2-carboxaldehyde. [M+H]+ calcd for C27H29N5O3S: 504.20; found: 503.99.

Sources & evidence

ORD record
ord-b39b4e1e242742cc9e970c93be912e72
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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