2-Chloro-6-trifluoromethylbenzothiazole → HCID 67521264, compound

HRID 667087Notes

Reaction equation

HRID 667087 reaction equation
[Cl:29][c:30]1[s:31][c:32]2[cH:33][c:34]([C:39]([F:40])([F:41])[F:42])[cH:35][cH:36][c:37]2[n:38]1.[F:1][c:2]1[cH:3][c:4]2[c:5]([n:6][c:7](-[c:9]3[c:10]([NH2:26])[n:11][cH:12][c:13](-[c:15]4[cH:16][n:17][n:18]([CH:20]5[CH2:21][CH2:22][NH:23][CH2:24][CH2:25]5)[cH:19]4)[cH:14]3)[s:8]2)[cH:27][cH:28]1>>[c:2]1([C:39]([F:40])([F:41])[F:42])[cH:3][c:4]2[c:5]([n:6][c:7](-[c:9]3[c:10]([NH2:26])[n:11][cH:12][c:13](-[c:15]4[cH:16][n:17][n:18]([CH:20]5[CH2:21][CH2:22][NH:23][CH2:24][CH2:25]5)[cH:19]4)[cH:14]3)[s:8]2)[cH:27][cH:28]1

Participants

3

Reactant 2

HCID 114704192-Chloro-6-trifluoromethylbenzothiazoleHCID 675210153-(6-fluorobenzothiazol-2-yl)-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-ylamine

Product 1

HCID 67521264HCID 67521264, compound

Sources & evidence

ORD record
ord-fdbac257ff31422fbf9973ae2d93825e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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