HCID 67265137, compound → HCID 178493696, compound

HRID 1132110Notes

Reaction equation

HRID 1132110 reaction equation
[CH3:1][O:2][c:3]1[c:4]([NH2:20])[cH:5][cH:6][c:7]2[c:8]1[CH2:9][CH2:10][CH2:11][CH:12]([N:14]1[CH2:15][CH2:16][O:17][CH2:18][CH2:19]1)[CH2:13]2.[Cl:21][c:22]1[n:23][cH:24][c:25]([Cl:40])[c:26]([NH:28][CH:29]2[CH:30]([NH:35][S:36](=[O:37])(=[O:38])[CH3:39])[CH2:31][CH2:32][CH2:33][CH2:34]2)[n:27]1>>[CH3:1][O:2][c:3]1[c:4]([NH:20][c:22]2[n:23][cH:24][c:25]([Cl:40])[c:26]([NH:28][CH:29]3[CH:30]([NH:35][S:36](=[O:37])(=[O:38])[CH3:39])[CH2:31][CH2:32][CH2:33][CH2:34]3)[n:27]2)[cH:5][cH:6][c:7]2[c:8]1[CH2:9][CH2:10][CH2:11][CH:12]([N:14]1[CH2:15][CH2:16][O:17][CH2:18][CH2:19]1)[CH2:13]2

Participants

3

Reactant 2

HCID 67265137HCID 67265137, compoundHCID 86633859N-[2-(2,5-dichloro-pyrimidin-4-ylamino)-cyclohexyl]-methanesulfonamide

Product 1

HCID 178493696HCID 178493696, compound

Sources & evidence

ORD record
ord-c729a673e0be41958f2a7bd69adce429
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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