Phenylboronic Acid → HCID 67259830, compound

HRID 2343520Notes

Reaction equation

HRID 2343520 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[n:6][n:7]2[c:8]([n:9][c:10]([CH3:22])[c:11]([CH:14]([C:15](=[O:16])[O:17][CH3:18])[CH2:19][CH2:20][CH3:21])[c:12]2[Cl:13])[cH:23]1.[CH:33]([N:34]([CH:35]([CH3:36])[CH3:37])[CH2:38][CH3:39])([CH3:40])[CH3:41].[OH:24][B:25]([OH:26])[c:27]1[cH:28][cH:29][cH:30][cH:31][cH:32]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[n:6][n:7]2[c:8]([n:9][c:10]([CH3:22])[c:11]([CH:14]([C:15](=[O:16])[O:17][CH3:18])[CH2:19][CH2:20][CH3:21])[c:12]2-[c:27]2[cH:28][cH:29][cH:30][cH:31][cH:32]2)[cH:23]1

Participants

4

Reactant 3

HCID 66827Phenylboronic AcidHCID 81531DiisopropylethylamineHCID 86674712Methyl 2-(2-tert-butyl-7-chloro-5-methylpyrazolo[1,5-a]pyrimidin-6-yl)pentanoate

Product 1

HCID 67259830HCID 67259830, compound

Sources & evidence

ORD record
ord-6266e541e5944329934c702a6ae80998
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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