4-Methyl-5-(2-hydroxyethyl)thiazole → HCID 69217389、化合物

HRID 272732

反応式

HRID 272732 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([O:9][CH3:10])[CH:3]=1.[CH3:11][C:12]1[N:13]=[CH:14][S:15][C:16]=1[CH2:17][CH2:18]O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1C=CC(COC(/N=N/C(OCC2C=CC=CC=2)=O)=O)=CC=1>C1COCC1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:18][CH2:17][C:16]2[S:15][CH:14]=[N:13][C:12]=2[CH3:11])=[C:4]([O:9][CH3:10])[CH:3]=1

参加物

6

実験手順

A mixture of 4-bromo-2-methoxy-phenol (50.8 mg, 0.25 mmol), 2-(4-methyl-thiazol-5-yl)-ethanol (49.5 mg, 0.25 mmol) and polymer-supported triphenyl phosphine (250 mg, 0.75 mmol) in THF (2.5 mL) was stirred at room temperature for 20 minutes. DBAD (86.3 mg, 0.375 mmol) was added and the mixture was stirred overnight at room temperature. The reaction mixture was filtered through Celite®, rinsing with THF and methanol. The filtrate was concentrated, diluted with ethyl acetate, washed with water and brine, dried (MgSO4), filtered and concentrated. The concentrate was purified by column chromatography on silica gel (10 to 20% ethyl acetate in hexane) to give the title compound. MS (ESI) m/e 329 (M+H)+; 1H NMR (300 MHz, DMSO-d6) □ 8.82 (s, 1H), 7.12 (d, J=2.4 Hz, 1H), 7.03 (dd, J=8.5, 2.4 Hz, 1H), 6.91 (d, J=8.5 Hz, 1H), 4.10 (t, J=6.4 Hz, 2H), 3.77 (s, 3H), 3.20 (t, J=6.4 Hz, 2H), 2.35 (s, 3H).

後処理

  1. stirringthe mixture was stirred overnight at room temperature
  2. filtrationThe reaction mixture was filtered through Celite®
  3. washrinsing with THF and methanol
  4. concentrationThe filtrate was concentrated
  5. additiondiluted with ethyl acetate
  6. washwashed with water and brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe concentrate was purified by column chromatography on silica gel (10 to 20% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-ed514b5f95dd4b72bf78e549e5649397
出典データセット
uspto-grants-2008_11
特許番号
US07456169B2

関連ノート

読み込み中…