2-Aminothiazole → HCID 25072940, compound

HRID 1550100Notes

Reaction equation

HRID 1550100 reaction equation
[CH3:38][O:39][CH2:40][CH2:41][O:42][CH3:43].[Cl:44][CH2:45][Cl:46].[NH2:32][c:33]1[s:34][cH:35][cH:36][n:37]1.[OH:1][c:2]1[c:3](-[c:19]2[cH:20][c:21]([C:22](=[O:23])[OH:24])[cH:25][cH:26][cH:27]2)[c:4]2[cH:5][cH:6][c:7](-[c:12]3[cH:13][c:14]([OH:18])[cH:15][cH:16][cH:17]3)[cH:8][c:9]2[cH:10][cH:11]1.[S:28]([Cl:29])([Cl:30])=[O:31]>>[OH:1][c:2]1[c:3](-[c:19]2[cH:20][c:21]([C:22](=[O:23])[NH:32][c:33]3[s:34][cH:35][cH:36][n:37]3)[cH:25][cH:26][cH:27]2)[c:4]2[cH:5][cH:6][c:7](-[c:12]3[cH:13][c:14]([OH:18])[cH:15][cH:16][cH:17]3)[cH:8][c:9]2[cH:10][cH:11]1

Participants

6

Reactant 5

HCID 21552-AminothiazoleHCID 6344DichloromethaneHCID 80711,2-DimethoxyethaneHCID 24386Thionyl ChlorideHCID 25069442HCID 25069442, compound

Product 1

HCID 25072940HCID 25072940, compound

Sources & evidence

ORD record
ord-3fefc0c66abb4234a54e99d5b9ecf323
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)

Reaction notes

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