5-Bromo-2-chloropyrimidine → HCID 21041370, compound

HRID 1128397Notes

Reaction equation

HRID 1128397 reaction equation
[Br:33][c:34]1[cH:35][n:36][c:37]([Cl:40])[n:38][cH:39]1.[Cl:1][c:2]1[c:3]([O:4][c:5]2[c:6]([NH:15][S:16]([NH:17][CH2:18][c:19]3[cH:20][cH:21][cH:22][cH:23][cH:24]3)(=[O:25])=[O:26])[n:7][cH:8][n:9][c:10]2[O:11][CH2:12][CH2:13][OH:14])[cH:27][c:28]([O:31][CH3:32])[cH:29][cH:30]1>>[Cl:1][c:2]1[c:3]([O:4][c:5]2[c:6]([NH:15][S:16]([NH:17][CH2:18][c:19]3[cH:20][cH:21][cH:22][cH:23][cH:24]3)(=[O:25])=[O:26])[n:7][cH:8][n:9][c:10]2[O:11][CH2:12][CH2:13][O:14][c:37]2[n:36][cH:35][c:34]([Br:33])[cH:39][n:38]2)[cH:27][c:28]([O:31][CH3:32])[cH:29][cH:30]1

Participants

3

Reactant 2

HCID 6066655-Bromo-2-chloropyrimidineHCID 21041229Benzylsulfamic acid [5-(2-chloro-5-methoxy-phenoxy)-6-(2-hydroxy-ethoxy) pyrimidin-4-yl]-amide

Product 1

HCID 21041370HCID 21041370, compound

Sources & evidence

ORD record
ord-3b9a82b295644a889d3331ed855724f8
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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