Chloride → HCID 71281430, compound

HRID 297674Notes

Reaction equation

HRID 297674 reaction equation
[C:1](#[N:2])[CH2:3][CH2:4][c:5]1[cH:6][cH:7][c:8]2[n:9]([cH:10]1)[c:11]([C:14](=[O:15])[OH:16])[cH:12][n:13]2.[CH3:54][N:55]([CH3:56])[CH:57]=[O:58].[Cl-:44].[Cl:17][C:18]([C:19]([Cl:20])=[O:21])=[O:22].[Cl:45][CH2:46][Cl:47].[NH2:23][c:24]1[cH:25][c:26](-[c:31]2[n:32][o:33][c:34]([CH:36]3[CH2:37][N:38]([C:40](=[O:41])[O:42][CH3:43])[CH2:39]3)[n:35]2)[cH:27][cH:28][c:29]1[CH3:30].[cH:48]1[cH:49][cH:50][n:51][cH:52][cH:53]1>>[C:1](#[N:2])[CH2:3][CH2:4][c:5]1[cH:6][cH:7][c:8]2[n:9]([cH:10]1)[c:11]([C:14](=[O:16])[NH:23][c:24]1[cH:25][c:26](-[c:31]3[n:32][o:33][c:34]([CH:36]4[CH2:37][N:38]([C:40](=[O:41])[O:42][CH3:43])[CH2:39]4)[n:35]3)[cH:27][cH:28][c:29]1[CH3:30])[cH:12][n:13]2

Participants

8

Reactant 7

HCID 312ChlorideHCID 1049PyridineHCID 6228DimethylformamideHCID 6344DichloromethaneHCID 65578Oxalyl chlorideHCID 712807766-(2-Cyanoethyl)imidazo[1,2-a]pyridine-3-carboxylic acidHCID 86677444Methyl 3-(3-(3-amino-4-methylphenyl)-1,2,4-oxadiazol-5-yl)azetidine-1-carboxylate

Product 1

HCID 71281430HCID 71281430, compound

Sources & evidence

ORD record
ord-8be33e97e8cb4315ada6eb9702315769
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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