Pyridine → Hydrochloric Acid

HRID 148772Notes

Reaction equation

HRID 148772 reaction equation
[C:1](#[N:2])[c:3]1[cH:4][cH:5][c:6]([C:7](=[O:8])[Cl:9])[cH:10][cH:11]1.[CH2:37]1[O:38][CH2:39][CH2:40][CH2:41]1.[NH2:12][c:13]1[c:14]([C:15](=[O:16])[NH:17][c:18]2[n:19][cH:20][c:21]([Cl:24])[cH:22][cH:23]2)[cH:25][c:26]([O:29][CH3:30])[cH:27][cH:28]1.[cH:31]1[cH:32][cH:33][n:34][cH:35][cH:36]1>>[C:1](#[N:2])[c:3]1[cH:4][cH:5][c:6]([C:7](=[O:8])[NH:12][c:13]2[c:14]([C:15](=[O:16])[NH:17][c:18]3[n:19][cH:20][c:21]([Cl:24])[cH:22][cH:23]3)[cH:25][c:26]([O:29][CH3:30])[cH:27][cH:28]2)[cH:10][cH:11]1.[ClH:9]

Participants

6

Reactant 4

HCID 1049PyridineHCID 8028TetrahydrofuranHCID 801724-Cyanobenzoyl chlorideHCID 219062412-amino-N-(5-chloropyridin-2-yl)-5-methoxybenzamide

Product 2

HCID 313Hydrochloric AcidHCID 22596384N-(5-chloropyridin-2-yl)-2-(4-cyanobenzamido)-5-methoxybenzamide

Sources & evidence

ORD record
ord-04381f4ffccb49bdbb81acb3d27769b8
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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