Isoindoline → HCID 58327812, compound

HRID 690640Notes

Reaction equation

HRID 690640 reaction equation
[CH2:32]1[NH:33][CH2:34][c:35]2[cH:36][cH:37][cH:38][cH:39][c:40]21.[Cl:1][c:2]1[cH:3][cH:4][c:5]([C:28]([F:29])([F:30])[F:31])[c:6]([CH2:7][N:8]2[c:9]3[c:10]([n:14][cH:15][c:16](-[c:18]4[cH:19][cH:20][c:21]([C:22](=[O:23])[OH:24])[cH:25][cH:26]4)[cH:17]3)[NH:11][CH2:12][CH2:13]2)[cH:27]1>>[Cl:1][c:2]1[cH:3][cH:4][c:5]([C:28]([F:29])([F:30])[F:31])[c:6]([CH2:7][N:8]2[c:9]3[c:10]([n:14][cH:15][c:16](-[c:18]4[cH:19][cH:20][c:21]([C:22](=[O:23])[N:33]5[CH2:32][c:40]6[c:35]([cH:36][cH:37][cH:38][cH:39]6)[CH2:34]5)[cH:25][cH:26]4)[cH:17]3)[NH:11][CH2:12][CH2:13]2)[cH:27]1

Participants

3

Reactant 2

HCID 422478IsoindolineHCID 469067184-{1-[5-Chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}benzoic acid

Product 1

HCID 58327812HCID 58327812, compound

Sources & evidence

ORD record
ord-4699a31687664e1a867da6d1b474b920
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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