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Triethylsilane → HCID 56974282、化合物

HRID 1417557
ノート
印刷プレビュー

反応式

HRID 1417557 の反応式
C([SiH](CC)CC)C.[CH3:8][O:9][C:10]([C@H:12]1[CH2:37][CH2:36][C@:14]2([O:18][CH:17]=[C:16]([C:19]3[CH:24]=[C:23]([N:25]4[CH:29]=[CH:28][N:27]=[C:26]4[C:30]([F:33])([F:32])[F:31])[CH:22]=[CH:21][C:20]=3[O:34][CH3:35])[CH2:15]2)[C@@H:13]1[C:38]1[CH:43]=[CH:42][C:41]([F:44])=[CH:40][CH:39]=1)=[O:11]>FC(F)(F)C(O)=O>[CH3:8][O:9][C:10]([C@H:12]1[CH2:37][CH2:36][C@:14]2([O:18][CH2:17][C@H:16]([C:19]3[CH:24]=[C:23]([N:25]4[CH:29]=[CH:28][N:27]=[C:26]4[C:30]([F:31])([F:32])[F:33])[CH:22]=[CH:21][C:20]=3[O:34][CH3:35])[CH2:15]2)[C@@H:13]1[C:38]1[CH:39]=[CH:40][C:41]([F:44])=[CH:42][CH:43]=1)=[O:11].[CH3:8][O:9][C:10]([C@H:12]1[CH2:37][CH2:36][C@:14]2([O:18][CH2:17][C@@H:16]([C:19]3[CH:24]=[C:23]([N:25]4[CH:29]=[CH:28][N:27]=[C:26]4[C:30]([F:31])([F:32])[F:33])[CH:22]=[CH:21][C:20]=3[O:34][CH3:35])[CH2:15]2)[C@@H:13]1[C:38]1[CH:39]=[CH:40][C:41]([F:44])=[CH:42][CH:43]=1)=[O:11]
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 2

HCID 12052TriethylsilaneHCID 67670838HCID 67670838、化合物

生成物 2

HCID 56974282HCID 56974282、化合物HCID 67670401HCID 67670401、化合物

試薬・触媒・溶媒 1

HCID 6422Trifluoroacetic acid溶媒

実験手順

Triethylsilane (0.0062 mL, 4.5 mg, 0.039 mmol) was added to a solution of (5R,6S,7S)-6-(4-fluorophenyl)-3-(2-methoxy-5-(2-(trifluoromethyl)imidazol-1-yl)phenyl)-1-oxaspiro[4.4]non-2-ene-7-carboxylic acid methyl ester (6.8 mg, 0.013 mmol) in 0.204 mL of trifluoroacetic acid at RT. The mixture was stirred 1 h at RT, then overnight at 60° C. After removing the solvent under reduced pressure, the residue was dissolved in 3.0 mL of ethyl acetate, washed with 2.0 mL of saturated aqueous sodium bicarbonate, dried over sodium sulfate and evaporated. The crude product was purified by preparative TLC, eluting twice with 3% ethyl ether in dichloromethane, to give 1.0 mg of (3S,5R,6S,7S)-6-(4-fluorophenyl)-3-(2-methoxy-5-(2-(trifluoromethyl)imidazol-1-yl)phenyl)-1-oxaspiro[4.4]nonane-7-carboxylic acid methyl ester and 2.6 mg of the title compound. 1NMR (400 MHz, CDCl3): δ 7.37 (dd, 2H, J=9, 6 Hz ), 7.19 (d, 1H, J=1 Hz), 7.15 (dd, 1H, J=9, 3 Hz ), 7.09 (d, 1H, J=2 Hz ), 7.08 (d, 1H, J=1 Hz ), 7.03 (t, 2H, J=9 Hz ), 6.82 (1H, J=9 Hz ), 3.78 (s, 3H), 3.70 (t, 1H, J=8 Hz ), 3.62 (t, 1H, J=8 Hz ), 3.56 (s, 3H), 3.14 (ddd, 1H, J=11, 10, 7 Hz ), 3.12 (d, 1H, J=11 Hz ), 2.87 (quintet, 1H, J=8 Hz ), 2.33-2.23 (m, 2H), 2.08-1.88 (m, 4H). Mass spectrum (ESI): m/z=519 (M+1).

後処理

  1. customovernight
  2. customat 60° C
  3. customAfter removing the solvent under reduced pressure
  4. dissolutionthe residue was dissolved in 3.0 mL of ethyl acetate
  5. washwashed with 2.0 mL of saturated aqueous sodium bicarbonate
  6. dry with materialdried over sodium sulfate
  7. customevaporated
  8. customThe crude product was purified by preparative TLC
  9. washeluting twice with 3% ethyl ether in dichloromethane

出典と根拠

ORDレコード
ord-cb7fdc7d2abc400eba347b001ab32efa
出典データセット
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05877191

反応ノート

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