Pyridine → HCID 22625670, compound

HRID 2318157Notes

Reaction equation

HRID 2318157 reaction equation
[C:1](=[O:2])([O:3][CH2:4][c:5]1[cH:6][cH:7][cH:8][cH:9][cH:10]1)[N:11]1[CH2:12][C:13]([c:15]2[c:16]([F:29])[cH:17][c:18]([N:21]3[C:22](=[O:28])[O:23][CH:24]([CH2:26][NH2:27])[CH2:25]3)[cH:19][cH:20]2)([CH3:30])[CH2:14]1.[CH3:37][C:38](=[O:39])[O:40][C:41](=[O:42])[CH3:43].[Cl:44][CH2:45][Cl:46].[cH:31]1[cH:32][cH:33][n:34][cH:35][cH:36]1>>[C:1](=[O:2])([O:3][CH2:4][c:5]1[cH:6][cH:7][cH:8][cH:9][cH:10]1)[N:11]1[CH2:12][C:13]([c:15]2[c:16]([F:29])[cH:17][c:18]([N:21]3[C:22](=[O:28])[O:23][CH:24]([CH2:26][NH:27][C:38]([CH3:37])=[O:39])[CH2:25]3)[cH:19][cH:20]2)([CH3:30])[CH2:14]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344DichloromethaneHCID 7918Acetic AnhydrideHCID 22625694HCID 22625694, compound

Product 1

HCID 22625670HCID 22625670, compound

Sources & evidence

ORD record
ord-b856caa48ef742228ee312c373f1e19d
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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