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Potassium bis(trimethylsilyl)amide → ethyl 4-methylene-7,8-dihydro-4H-thieno[2,3-d]azepine-6(5H)-carboxylate

HRID 1019608
ノート
印刷プレビュー

反応式

HRID 1019608 の反応式
[CH3:1][Si]([N-][Si](C)(C)C)(C)C.[K+].[CH2:11]([O:13][C:14]([N:16]1[CH2:22][C:21](=O)[C:20]2[CH:24]=[CH:25][S:26][C:19]=2[CH2:18][CH2:17]1)=[O:15])[CH3:12]>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1COCC1>[CH2:11]([O:13][C:14]([N:16]1[CH2:22][C:21](=[CH2:1])[C:20]2[CH:24]=[CH:25][S:26][C:19]=2[CH2:18][CH2:17]1)=[O:15])[CH3:12]
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

5

反応物 2

HCID 3251421Potassium bis(trimethylsilyl)amideHCID 574239834-Oxo-4,5,7,8-tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester

生成物 1

HCID 58293774ethyl 4-methylene-7,8-dihydro-4H-thieno[2,3-d]azepine-6(5H)-carboxylate収率 87.6%

試薬・触媒・溶媒 2

HCID 74505Methyltriphenyliphosphonium bromide触媒HCID 8028Tetrahydrofuran
溶媒
2 回

反応条件

温度
0 °C

実験手順

Methyl triphenylphosphonium bromide (6.3 g, 17.6 mmol) was dissolved in 150 mL THF and cooled to 0° C. KHMDS (3.2 g, 16.2 mmol) was added portionwise and the reaction was stirred for ½ hour. The product of Example 1, step (c) (3.0 g, 12.5 mmol) was added as a solution in 25 mL THF. The reaction was warmed to room temperature and stirred for 1 hour. The mixture was concentrated and the title product was purified by silica gel chromatography (0% to 40% EtOAc in hexanes) to give 2.6 g of the sub-title compound.

後処理

  1. temperatureThe reaction was warmed to room temperature
  2. stirringstirred for 1 hour
  3. concentrationThe mixture was concentrated
  4. customthe title product was purified by silica gel chromatography (0% to 40% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-169b7758fec74516be129d1fa1deb78f
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08716276B2

反応ノート

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