Pyridine → HCID 178429991, compound

HRID 1151068Notes

Reaction equation

HRID 1151068 reaction equation
[CH3:1][c:2]1[cH:3][n:4]([CH:5]2[CH2:6][CH:7]([OH:8])[CH:9]([CH2:10][OH:11])[O:12]2)[c:13](=[O:14])[nH:15][c:16]1=[O:17].[Cl:24][c:25]1[cH:26][c:27]([N+:37](=[O:38])[O-:39])[c:28]([CH2:31][CH2:32][O:33][C:34](=[O:35])[Cl:36])[cH:29][cH:30]1.[Cl:40][CH2:41][Cl:42].[cH:18]1[cH:19][cH:20][n:21][cH:22][cH:23]1>>[CH3:1][c:2]1[cH:3][n:4]([CH:5]2[CH2:6][CH:7]([OH:8])[CH:9]([CH2:10][O:11][C:34]([O:33][CH2:32][CH2:31][c:28]3[c:27]([N+:37](=[O:38])[O-:39])[cH:26][c:25]([Cl:24])[cH:30][cH:29]3)=[O:35])[O:12]2)[c:13](=[O:14])[nH:15][c:16]1=[O:17]

Participants

5

Reactant 4

HCID 1049PyridineHCID 11341-(2-Deoxypentofuranosyl)-4-hydroxy-5-methylpyrimidin-2(1H)-oneHCID 6344DichloromethaneHCID 190827062-(4-Chloro-2-nitrophenyl)ethoxycarbonyl chloride

Product 1

HCID 178429991HCID 178429991, compound

Sources & evidence

ORD record
ord-2a8cb8e084a342e199add767db120a89
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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