p-Anisoyl chloride → 2-Amino-4-(2-furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazole
Reaction equation
[CH3:1][O:2][c:3]1[cH:4][cH:5][c:6]([C:7]([Cl:8])=[O:9])[cH:10][cH:11]1.[o:12]1[c:13](-[c:17]2[n:18][c:19]([NH:30][C:31](=[O:32])[c:33]3[cH:34][cH:35][c:36]([O:37][CH3:38])[cH:39][cH:40]3)[s:20][c:21]2[C:22](=[O:23])[CH:24]2[CH2:25][CH2:26][O:27][CH2:28][CH2:29]2)[cH:14][cH:15][cH:16]1>>[o:12]1[c:13](-[c:17]2[n:18][c:19]([NH2:30])[s:20][c:21]2[C:22](=[O:23])[CH:24]2[CH2:25][CH2:26][O:27][CH2:28][CH2:29]2)[cH:14][cH:15][cH:16]1Participants
3
Sources & evidence
- ORD record
- ord-bfa9b134fa5942c6a07f7caab0440d3a
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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