Phenylboronic Acid → HCID 67312064, compound

HRID 135705Notes

Reaction equation

HRID 135705 reaction equation
[Cl:1][c:2]1[c:3]2[c:4]([n:5][c:6]([NH2:8])[n:7]1)[n:9]([CH2:12][c:13]1[n:14][c:15]([CH2:19][O:20][CH:21]3[CH2:22][O:23][CH2:24][CH2:25]3)[cH:16][cH:17][cH:18]1)[n:10][n:11]2.[OH:26][B:27]([OH:28])[c:29]1[cH:30][cH:31][cH:32][cH:33][cH:34]1>>[c:2]1(-[c:29]2[cH:30][cH:31][cH:32][cH:33][cH:34]2)[c:3]2[c:4]([n:5][c:6]([NH2:8])[n:7]1)[n:9]([CH2:12][c:13]1[n:14][c:15]([CH2:19][O:20][CH:21]3[CH2:22][O:23][CH2:24][CH2:25]3)[cH:16][cH:17][cH:18]1)[n:10][n:11]2

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 871224007-Chloro-3-[[6-(oxolan-3-yloxymethyl)-2-pyridinyl]methyl]triazolo[4,5-d]pyrimidin-5-amine

Product 1

HCID 67312064HCID 67312064, compound

Sources & evidence

ORD record
ord-25ea37fca13240a7b3751a75363e1250
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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