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Borane → HCID 67087005、化合物

HRID 2365536
ノート
印刷プレビュー

反応式

HRID 2365536 の反応式
[NH2:1][C@H:2]([CH2:6][CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][Si](C(C)(C)C)(C)C)=[CH:11][CH:10]=1)[C:3]([NH2:5])=O.B>C1COCC1.CO>[NH2:1][C@@H:2]([CH2:3][NH2:5])[CH2:6][CH2:7][CH2:8][C:9]1[CH:10]=[CH:11][C:12]([OH:15])=[CH:13][CH:14]=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

5

反応物 2

HCID 6331Borane3 回HCID 67087069HCID 67087069、化合物

生成物 1

HCID 67087005HCID 67087005、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒4 回

反応条件

温度
5 °C

実験手順

A solution of (R)-2-Amino-5-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-pentanoic acid amide (7.74 g, 24 mmol) in THF is stirred at 5° C. and borane (96 ml of a 1 M solution in THF, 96 mmol) is added. The mixture is stirred at 5° C. until a homogeneous mixture is obtained and then stirred at room temperature for 30 minutes and 35° C. for 3 hours. After this time, further borane (24 ml of a 1 M solution in THF, 24 mmol) is added and the reaction is heated at 35° C. for 18 hours. After this time, a further portion of borane (24 ml of a 1 M solution in THF, 24 mmol) is added and the reaction heated at 35° C. for a further 24 hours. After this time, the reaction is cooled to 10° C., and quenched by adding dropwise to MeOH (50 ml) at −5° C. After allowing to warm to room temperature the solvent is removed in vacuo to afford a yellow oil. The oil is dissolved in MeOH (250 ml) and SCX-2 silica (180 g, 0.63 mmol/g, 120 mmol) is added. The silica suspension is shaken for 18 hours, the silica is removed by filtration, washed with MeOH (3×100 ml), then suspended in 7M NH3 in MeOH and shaken for 18 hours. The silica is removed by filtration and the 7M NH3 in MeOH is removed in vacuo to afford the title compound as a yellow oil; [M+H]+ 195

後処理

  1. customis obtained
  2. stirringstirred at room temperature for 30 minutes and 35° C. for 3 hours
  3. temperaturethe reaction is heated at 35° C. for 18 hours
  4. temperaturethe reaction heated at 35° C. for a further 24 hours
  5. temperatureAfter this time, the reaction is cooled to 10° C.
  6. customquenched
  7. additionby adding dropwise to MeOH (50 ml) at −5° C
  8. temperatureto warm to room temperature the solvent
  9. customis removed in vacuo
  10. customto afford a yellow oil
  11. additionSCX-2 silica (180 g, 0.63 mmol/g, 120 mmol) is added
  12. stirringThe silica suspension is shaken for 18 hours
  13. customthe silica is removed by filtration
  14. washwashed with MeOH (3×100 ml)
  15. stirringshaken for 18 hours
  16. customThe silica is removed by filtration
  17. customthe 7M NH3 in MeOH is removed in vacuo

出典と根拠

ORDレコード
ord-08955a9456d141e9b801610cf6518fba
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08697687B2

反応ノート

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