2-Aminothiazole → HCID 24889765, compound

HRID 2126049Notes

Reaction equation

HRID 2126049 reaction equation
[CH3:31][O:32][c:33]1[cH:34][c:35](-[c:39]2[c:40]3[c:41]([n:42][c:43]([N:45]4[CH2:46][CH2:47][O:48][CH2:49][CH2:50]4)[n:44]2)[N:51]([c:54]2[s:55][cH:56][cH:57][n:58]2)[CH2:52][CH2:53]3)[cH:36][cH:37][cH:38]1.[Cl:1][c:2]1[c:3]([CH2:4][CH2:5][Cl:6])[c:7](-[c:8]2[cH:9][cH:10][cH:11][c:12]([O:13][CH3:14])[cH:15]2)[n:16][c:17]([N:18]2[CH2:19][CH2:20][O:21][CH2:22][CH2:23]2)[n:24]1.[NH2:25][c:26]1[s:27][cH:28][cH:29][n:30]1>>[OH:32][c:33]1[cH:34][c:35](-[c:39]2[c:40]3[c:41]([n:42][c:43]([N:45]4[CH2:46][CH2:47][O:48][CH2:49][CH2:50]4)[n:44]2)[N:51]([c:54]2[s:55][cH:56][cH:57][n:58]2)[CH2:52][CH2:53]3)[cH:36][cH:37][cH:38]1

Participants

4

Reactant 3

HCID 21552-AminothiazoleHCID 592449884-[4-Chloro-5-(2-chloroethyl)-6-(3-methoxyphenyl)-pyrimidin-2-yl]morpholineHCID 67386637HCID 67386637, compound

Product 1

HCID 24889765HCID 24889765, compound

Sources & evidence

ORD record
ord-51495bd82be64578919986b134322966
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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