Bromotrimethylsilane → HCID 178485583, Verbindung

HRID 2279815Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2279815
[OH:1][CH2:2][CH2:3][CH2:4][N:5]1[CH:9]=[C:8]([C:10]2[N:15]=[C:14]([C:16](=[O:19])[NH:17][CH3:18])[C:13]([NH:20][C:21]3[C:26]([C:27]([F:30])([F:29])[F:28])=[CH:25][N:24]=[C:23]([NH:31][C:32]4[CH:46]=[CH:45][C:35]([CH2:36][CH2:37][CH2:38][CH2:39][PH:40](=[O:44])[O:41]CC)=[CH:34][C:33]=4[O:47][CH3:48])[N:22]=3)=[CH:12][CH:11]=2)[CH:7]=[N:6]1.Br[Si](C)(C)C>N1C=CC=CC=1>[OH:1][CH2:2][CH2:3][CH2:4][N:5]1[CH:9]=[C:8]([C:10]2[N:15]=[C:14]([C:16](=[O:19])[NH:17][CH3:18])[C:13]([NH:20][C:21]3[C:26]([C:27]([F:29])([F:30])[F:28])=[CH:25][N:24]=[C:23]([NH:31][C:32]4[CH:46]=[CH:45][C:35]([CH2:36][CH2:37][CH2:38][CH2:39][PH:40](=[O:41])[OH:44])=[CH:34][C:33]=4[O:47][CH3:48])[N:22]=3)=[CH:12][CH:11]=2)[CH:7]=[N:6]1

Komponenten

4

Versuchsvorschrift

A solution of ethyl (4-{[4-({6-[1-(3-hydroxypropyl)-1H-pyrazol-4-yl]-2-(methylcarbamoyl)pyridin-3-yl}amino)-5-(trifluoromethyl)pyrimidin-2-yl]amino}-3-methoxybenzyl)propylphosphinate (Compound 37B, 10 mg, 0.015 mmol) in pyridine (1 mL) was charged with bromotrimethylsilane (0.012 mL, 0.087 mmol). The reaction was stirred at rt for 20 min. The material was not isolated. MS (ESI): m/z 663.23 [M+H]+. UPLC: tR=0.85 min (polar—2 min).

Aufarbeitung

  1. customThe material was not isolated
  2. customtR=0.85 min (polar—2 min)

Quellen und Nachweise

ORD-Eintrag
ord-1564163956224e7d88eaccf279d71af0
Quelldatensatz
uspto-grants-2015_09
Patentnummer
US09133224B2

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