Phenylboronic Acid → HCID 24871617, compound

HRID 174252Notes

Reaction equation

HRID 174252 reaction equation
[C:1]([O:2][C:3](=[O:4])[N:8]1[CH2:9][CH2:10][c:11]2[c:12](-[c:28]3[cH:29][cH:30][cH:31][cH:32][cH:33]3)[n:13](-[c:18]3[cH:19][c:20]([C:24]([F:25])([F:26])[F:27])[cH:21][cH:22][cH:23]3)[n:14][c:15]2[CH2:16][CH2:17]1)([CH3:5])([CH3:6])[CH3:7].[C:34]([O:35][C:36]([N:37]1[CH2:38][CH2:39][c:40]2[c:41]([c:42]([O:43][S:44]([C:45]([F:46])([F:47])[F:48])(=[O:49])=[O:50])[n:51](-[c:52]3[cH:53][cH:54][cH:55][c:56]([C:57]([F:58])([F:59])[F:60])[cH:61]3)[n:62]2)[CH2:63][CH2:64]1)=[O:65])([CH3:66])([CH3:67])[CH3:68].[OH:69][B:70]([c:71]1[cH:72][cH:73][cH:74][cH:75][cH:76]1)[OH:77]>>[NH:8]1[CH2:9][CH2:10][c:11]2[c:12](-[c:28]3[cH:29][cH:30][cH:31][cH:32][cH:33]3)[n:13](-[c:18]3[cH:19][c:20]([C:24]([F:25])([F:26])[F:27])[cH:21][cH:22][cH:23]3)[n:14][c:15]2[CH2:16][CH2:17]1

Participants

4

Reactant 3

HCID 66827Phenylboronic AcidHCID 67268842HCID 67268842, compoundHCID 86598386HCID 86598386, compound

Product 1

HCID 24871617HCID 24871617, compound

Sources & evidence

ORD record
ord-c5581763fe4f4f1ea007d85157d8ac1a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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