Pyridine → HCID 23369364, compound

Reaction equation

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

Participants

Reactant 4

HCID 1049Pyridine

HCID 6344Dichloromethane

HCID 7918Acetic Anhydride

HCID 23369362HCID 23369362, compound

Product 1

HCID 23369364HCID 23369364, compound

Sources & evidence

ORD record: ord-15ddf564343b48c080c477e0e1aa8cce
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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