(Pyrimidin-5-yl)boronic acid → HCID 118195193, compound

HRID 924067Notes

Reaction equation

HRID 924067 reaction equation
Br[C:2]1[C:3]([N:23]2[CH2:27][CH2:26][C@@H:25]([OH:28])[CH2:24]2)=[N:4][CH:5]=[C:6]([CH:22]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([S:16][C:17]([F:20])([F:19])[F:18])=[C:12]([F:21])[CH:11]=1)=[O:8].[N:29]1[CH:34]=[C:33](B(O)O)[CH:32]=[N:31][CH:30]=1>>[F:21][C:12]1[CH:11]=[C:10]([NH:9][C:7](=[O:8])[C:6]2[CH:22]=[C:2]([C:33]3[CH:34]=[N:29][CH:30]=[N:31][CH:32]=3)[C:3]([N:23]3[CH2:27][CH2:26][C@@H:25]([OH:28])[CH2:24]3)=[N:4][CH:5]=2)[CH:15]=[CH:14][C:13]=1[S:16][C:17]([F:20])([F:19])[F:18]

Participants

3

Procedure

The title compound was prepared in an analogous fashion to that described in Example 185 using (R)-5-bromo-N-(3-fluoro-4-((trifluoromethyl)thio)phenyl)-6-(3-hydroxypyrrolidin-1-yl)nicotinamide (Stage 205.1) and pyrimidin-5-ylboronic acid to afford a white powder. HPLC (Condition 4) tR=5.22 min, UPLC-MS (Condition 3) tR=1.03 min, m/z=480.2 [M+H]+; 1H-NMR (400 MHz, DMSO-d6) δ ppm 1.67-1.77 (m, 1H) 1.79-1.94 (m, 1H) 2.82-2.94 (m, 1H) 3.22 (m, J=11.10, 4.10 Hz, 2H) 3.32-3.45 (m, 1H) 4.14-4.29 (m, 1H) 4.87 (d, J=3.91 Hz, 1H) 7.58-7.80 (m, 2H) 7.96 (dd, J=11.73, 1.96 Hz, 1H) 8.08 (d, J=2.35 Hz, 1H) 8.79 (d, J=2.35 Hz, 1H) 8.88 (s, 2H) 9.18 (s, 1H) 10.43 (s, 1H).

Workup

  1. customto afford a white powder

Sources & evidence

ORD record
ord-fc816f6db29c49a9a099fa8af54cb62e
Source dataset
uspto-grants-2016_03
Patent number
US09278981B2

Reaction notes

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