Ethanesulfonyl chloride → HCID 49773318, compound

HRID 306389Notes

Reaction equation

HRID 306389 reaction equation
[CH2:28]([CH3:29])[S:30](=[O:31])(=[O:32])[Cl:33].[NH2:1][c:2]1[n:3][c:4]([O:5][CH2:6][CH3:7])[c:8]2[n:9][c:10](-[c:11]3[cH:12][c:13]([NH:14][S:15]([CH:16]([CH3:17])[CH3:18])(=[O:19])=[O:20])[cH:21][cH:22][cH:23]3)[cH:24][cH:25][c:26]2[n:27]1.[NH2:34][c:35]1[cH:36][cH:37][c:38](-[c:41]2[cH:42][cH:43][c:44]3[n:45][c:46]([NH2:54])[n:47][c:48]([O:51][CH2:52][CH3:53])[c:49]3[n:50]2)[cH:39][cH:40]1>>[CH2:28]([CH3:29])[S:30](=[O:31])(=[O:32])[NH:34][c:35]1[cH:36][cH:37][c:38](-[c:41]2[cH:42][cH:43][c:44]3[n:45][c:46]([NH2:54])[n:47][c:48]([O:51][CH2:52][CH3:53])[c:49]3[n:50]2)[cH:39][cH:40]1

Participants

4

Reactant 3

HCID 11667Ethanesulfonyl chlorideHCID 24959620HCID 24959620, compoundHCID 580198026-(4-Aminophenyl)-4-ethoxypyrido[3,2-d]pyrimidin-2-amine

Product 1

HCID 49773318HCID 49773318, compound

Sources & evidence

ORD record
ord-f7861f54c8e744748b9ebdfb6357dd96
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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