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Pyridine → HCID 23144205, compound

HRID 2326303
Notes
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Reaction equation

HRID 2326303 reaction equation
[CH3:1][N:2]([C:3](=[O:4])[N:5]1[CH2:6][CH2:7][CH:8]([C:11](=[O:12])[OH:13])[CH2:9][CH2:10]1)[CH3:14].[Cl:42][CH2:43][Cl:44].[NH2:25][c:26]1[s:27][c:28]([N:36]2[CH2:37][CH2:38][O:39][CH2:40][CH2:41]2)[c:29](-[c:31]2[o:32][cH:33][cH:34][cH:35]2)[n:30]1.[S:15]([Cl:16])([Cl:17])=[O:18].[cH:19]1[cH:20][cH:21][n:22][cH:23][cH:24]1>>[CH3:1][N:2]([C:3](=[O:4])[N:5]1[CH2:6][CH2:7][CH:8]([C:11](=[O:13])[NH:25][c:26]2[s:27][c:28]([N:36]3[CH2:37][CH2:38][O:39][CH2:40][CH2:41]3)[c:29](-[c:31]3[o:32][cH:33][cH:34][cH:35]3)[n:30]2)[CH2:9][CH2:10]1)[CH3:14]
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 1049PyridineHCID 6344DichloromethaneHCID 24386Thionyl ChlorideHCID 50764741-(dimethylcarbamoyl)piperidine-4-carboxylic acidHCID 231441582-Amino-4-(2-furyl)-5-morpholinothiazole

Product 1

HCID 23144205HCID 23144205, compound

Sources & evidence

ORD record
ord-c11df88f74974132a746efcc0cdbaa66
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes