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Methyl iodide → HCID 57270309、化合物

HRID 1417553
ノート
印刷プレビュー

反応式

HRID 1417553 の反応式
C[Si]([N-][Si](C)(C)C)(C)C.[Na+].C(OC([NH:21][C@H:22]1[CH2:47][CH2:46][C@:24]2([O:28][CH2:27][C@H:26]([C:29]3[CH:34]=[C:33]([N:35]4[CH:39]=[CH:38][N:37]=[C:36]4[C:40]([F:43])([F:42])[F:41])[CH:32]=[CH:31][C:30]=3[O:44][CH3:45])[CH2:25]2)[C@@H:23]1[C:48]1[CH:53]=[CH:52][C:51]([F:54])=[CH:50][CH:49]=1)=O)C1C=CC=CC=1.IC.[C:57]([O:60][CH2:61][CH3:62])(=[O:59])[CH3:58]>C1COCC1>[CH2:61]([O:60][C:57]([CH2:58][NH:21][C@H:22]1[CH2:47][CH2:46][C@:24]2([O:28][CH2:27][C@H:26]([C:29]3[CH:34]=[C:33]([N:35]4[CH:39]=[CH:38][N:37]=[C:36]4[C:40]([F:42])([F:43])[F:41])[CH:32]=[CH:31][C:30]=3[O:44][CH3:45])[CH2:25]2)[C@@H:23]1[C:48]1[CH:49]=[CH:50][C:51]([F:54])=[CH:52][CH:53]=1)=[O:59])[C:62]1[CH:46]=[CH:47][CH:22]=[CH:23][CH:24]=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

6

反応物 4

HCID 6328Methyl iodideHCID 8857Ethyl AcetateHCID 2724254Sodium bis(trimethylsilyl)amideHCID 67670349HCID 67670349、化合物

生成物 1

HCID 57270309HCID 57270309、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

A THF solution of sodium bis(trimethylsily)amide (0.059 mL, 1.0M, 0.059 mmol) was added to an ice-cooled solution of (3S,5R,6R,7S)-7-(benzyloxycarbonylamino)-6-(4-fluorophenyl)-3-(2-methoxy-5-(2-(trifluoromethyl)imidazol-1-yl)phenyl)-1-oxaspiro[4.4]nonane (30 mg, 0.049 mmol) in 0.50 mL of dry THF. After stirring for 15 minutes at 0° C., iodomethane (0.0037 mL, 8.4 mg, 0.059 mmol) was added. The mixture was stirred at 0° C., then allowed to warm up to RT for 3 h. The reaction was diluted in 20 mL of ethyl acetate and washed with 10 mL of saturated aqueous sodium bicarbonate, followed by 10 mL of brine. Drying over sodium sulfate and concentration afforded the crude product. Purification by preparative TLC, eluting with 30% ethyl ether in 1:1 toluene/hexane, yielded 7.5 mg of pure title compound and 15 mg of a mixture containing the title compound and recovered starting material. Mass spectrum (NH3/CI): m/z=624.2 (M+1).

後処理

  1. stirringThe mixture was stirred at 0° C.
  2. temperatureto warm up to RT for 3 h
  3. washwashed with 10 mL of saturated aqueous sodium bicarbonate
  4. dry with materialDrying over sodium sulfate and concentration
  5. customafforded the crude product
  6. customPurification by preparative TLC
  7. washeluting with 30% ethyl ether in 1:1 toluene/hexane

出典と根拠

ORDレコード
ord-fd1ef373e2cd4d4ba1e33f89a23b3c8d
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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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート