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Propanal → (S)-10-[3-(2-Methoxy-ethyl)-4-propyl-piperazin-1-yl]-2-trifluoromethyl-4H-3-thia-1,4,9-triaza-benzo[f]azulene

HRID 131503
ノート
印刷プレビュー

反応式

HRID 131503 の反応式
C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[CH:15](=O)[CH2:16][CH3:17].[CH3:19][O:20][CH2:21][CH2:22][C@@H:23]1[NH:28][CH2:27][CH2:26][N:25]([C:29]2[C:38]3[N:37]=[C:36]([C:39]([F:42])([F:41])[F:40])[S:35][C:34]=3[NH:33][C:32]3[CH:43]=[CH:44][CH:45]=[CH:46][C:31]=3[N:30]=2)[CH2:24]1>ClC(Cl)C>[CH3:19][O:20][CH2:21][CH2:22][C@@H:23]1[N:28]([CH2:15][CH2:16][CH3:17])[CH2:27][CH2:26][N:25]([C:29]2[C:38]3[N:37]=[C:36]([C:39]([F:41])([F:42])[F:40])[S:35][C:34]=3[NH:33][C:32]3[CH:43]=[CH:44][CH:45]=[CH:46][C:31]=3[N:30]=2)[CH2:24]1
参加物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 527PropanalHCID 5049666Sodium triacetoxyborohydrideHCID 135457486(S)-10-[3-(2-Methoxy-ethyl)-piperazin-1-yl]-2-trifluoromethyl-4H-3-thia-1,4,9-triaza-benzo[f]azulene

生成物 1

HCID 136090397(S)-10-[3-(2-Methoxy-ethyl)-4-propyl-piperazin-1-yl]-2-trifluoromethyl-4H-3-thia-1,4,9-triaza-benzo[f]azulene収率 74%

試薬・触媒・溶媒 1

HCID 6365
1,1-Dichloroethane
溶媒

実験手順

Add sodium triacetoxyborohydride (0.273 g, 1.29 mmol), and then propionaldehyde (0.083 mL, 1.15 mmol) to (S)-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-2-trifluoromethyl-4H-3-thia-1,4,9-triaza-benzo[f]azulene (0.353 g, 0.858 mmol) in anhydrous dichloroethane (15 mL) and stir at ambient temperature overnight. Add saturated aqueous sodium bicarbonate and extract aqueous phase with dichloromethane. Wash organics with saturated aqueous sodium chloride, and dry (sodium sulfate), filter, and concentrate under reduced pressure to a residue (0.29 g). Purify the residue by flash chromatography, eluting with a gradient of a 3% solution of 2M ammonia in methanol, in dichloromethane, (0-100%) to give the title compound (0.287 g, 74%): mass spectrum (APCI, m/e): 454 (M+1); NMR (1H, 300 MHz, DMSO-d6): δ 8.46 (s, 1H), 6.96-6.82 (m, 3H), 6.71 (m, 1H), 3.46 (br. m, 3H), 3.31-3.17 (m, 3H), 3.15 (s, 3H), 2.73 (m, 1H), 2.58-2.44 (m, 2H), 2.31 (m, 2H), 1.67 (m, 2H), 1.40 (m, 2H), 0.83 (t, 3H, J=7.5 Hz).

後処理

  1. extractionAdd saturated aqueous sodium bicarbonate and extract aqueous phase with dichloromethane
  2. dry with materialWash organics with saturated aqueous sodium chloride, and dry (sodium sulfate)
  3. filtrationfilter
  4. concentrationconcentrate under reduced pressure to a residue (0.29 g)
  5. customPurify the residue by flash chromatography
  6. washeluting with a gradient of a 3% solution of 2M ammonia in methanol, in dichloromethane, (0-100%)

出典と根拠

ORDレコード
ord-9e84d0cc3eb64360aa62c459bd2fda8e
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07384934B2

反応ノート

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