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3-Bromobenzyl alcohol → 2-(3-Bromobenzyloxy)-5-fluoropyrimidin-4-ylamine

HRID 705558
ノート
印刷プレビュー

反応式

HRID 705558 の反応式
CC([O-])(C)C.[K+].[Br:7][C:8]1[CH:9]=[C:10]([CH2:14][OH:15])[CH:11]=[CH:12][CH:13]=1.Cl[C:17]1[N:22]=[C:21]([NH2:23])[C:20]([F:24])=[CH:19][N:18]=1>O>[Br:7][C:8]1[CH:9]=[C:10]([CH:11]=[CH:12][CH:13]=1)[CH2:14][O:15][C:17]1[N:22]=[C:21]([NH2:23])[C:20]([F:24])=[CH:19][N:18]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 851413-Bromobenzyl alcoholHCID 2543722-Chloro-5-fluoropyrimidin-4-amineHCID 23665647Potassium tert-butoxide

生成物 1

HCID 578188342-(3-Bromobenzyloxy)-5-fluoropyrimidin-4-ylamine収率 49.3%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
90 °C

実験手順

To a magnetically stirred mixture of KOtBu (1.0 M in tBuOH, 1.36 ml, 1.36 mmol) was added (3-bromophenyl)methanol (0.25 g, 1.36 mmol). To the resulting solution was added 2-chloro-5-fluoropyrimidine-4-ylamine (0.10 g, 0.68 mmol) and the mixture was capped and stirred at 90° C. for 4 h. The reaction mixture was cooled to room temperature, diluted with water, and the resulting precipitate was collected by filtration. The solid was washed with water, washed with cyclohexane, and dried in the vacuum oven. A CH2Cl2 solution of the compound was loaded onto Biotage SCX column and eluted with CH2Cl2 followed by 2.0 M NH3 in MeOH. The solvent was evaporated under reduced pressure to give the title compound (0.100 g, 49%) as an off-white solid: mp 143-145° C.; 1H NMR (400 MHz, DMSO-d6) δ 7.90 (d, J=2.5 Hz, 1H), 7.61 (s, 1H), 7.43 (d, J=8.0 Hz, 1H), 7.36 (d, J=7.7 Hz, 1H), 7.22 (t, J=7.7 Hz, 1H), 5.28 (s, 2H), 5.20 (br s, 2H); GCMS (EI) m/z 297, 299 (M)+.

後処理

  1. customthe mixture was capped
  2. temperatureThe reaction mixture was cooled to room temperature
  3. filtrationthe resulting precipitate was collected by filtration
  4. washThe solid was washed with water
  5. washwashed with cyclohexane
  6. customdried in the vacuum oven
  7. washeluted with CH2Cl2
  8. customThe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-974a0a9392874bb184fb5a37f029953f
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09174970B2

反応ノート

読み込み中…

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