Diethyl Ether → HCID 178437119、化合物

HRID 630152ノート

反応式

HRID 630152 の反応式
Br[CH2:2][C:3]1[C:8]([CH2:9][CH3:10])=[CH:7][N:6]=[CH:5][C:4]=1[CH2:11][CH3:12].[SH:13][C:14]1[N:19]=[C:18]([OH:20])[CH:17]=[C:16]([C:21](F)(F)F)[N:15]=1.C(N(CC)CC)C.CCOCC>C(O)C>[CH2:11]([C:4]1[CH:5]=[N:6][CH:7]=[C:8]([CH2:9][CH3:10])[C:3]=1[CH2:2][S:13][C:14]1[N:19]=[C:18]([OH:20])[CH:17]=[C:16]([CH3:21])[N:15]=1)[CH3:12].[CH2:9]([C:8]1[CH:7]=[N:6][CH:5]=[CH:4][C:3]=1[CH2:2][S:13][C:14]1[N:19]=[C:18]([OH:20])[CH:17]=[C:16]([CH3:21])[N:15]=1)[CH3:10]

参加物

7

実験手順

To a mixture of crude 4-(bromomethyl)-3,5-diethylpyridine and 2-sulfanyl-6-(trifluromethyl)pyrimidin-4-ol (0.838 g, 5.89 mmol) in anhydrous ethanol (50 mL) at 0° C. was added triethylamine (3.21 g, 4.42 mL, 31.75 mmol). The reaction mixture was allowed to stir at room temperature overnight. The solvent was evaporated to provide a crude residue. Ether was added to precipitate the triethylamine hydrobromide salt. The solid was filtered and washed with ether several times. The combined ether layers were evaporated, and the crude residue was purified by Combiflash using 0-10% MeOH in dichloromethane to provide 2-{[(3,5-diethylpyridin-4-yl)methyl]sulfanyl}-6-methylpyrimidin-4-ol and 2-{[(3-ethylpyridin-4-yl)methyl]sulfanyl}-6-methylpyrimidin-4-ol as a white solid; 1H NMR (400 MHz, DMSO-d6): δ 1.19 (t, 6H), 2.64 (q, 4H), 4.55 (s, 2H), 6.70 (s, 1H), 8.30 (s, 2H); M+1 344.4.

後処理

  1. customThe solvent was evaporated
  2. customto provide a crude residue
  3. customto precipitate the triethylamine hydrobromide salt
  4. filtrationThe solid was filtered
  5. washwashed with ether several times
  6. customThe combined ether layers were evaporated
  7. customthe crude residue was purified by Combiflash

出典と根拠

ORDレコード
ord-4b220a86f14e4f1ab6f1a8a542fb22cd
出典データセット
uspto-grants-2016_04
特許番号
US09315521B2

反応ノート

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