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Sodium borohydride → N-(2-ethyl-7-(2-methyl-4-nitro-pyrazol-3-yl)oxepan-4-yl)-2-methyl-propane-2-sulfinamide

HRID 521839
ノート
印刷プレビュー

反応式

HRID 521839 の反応式
[CH2:1]([CH:3]1[CH2:9][C:8](=O)[CH2:7][CH2:6][CH:5]([C:11]2[N:12]([CH3:19])[N:13]=[CH:14][C:15]=2[N+:16]([O-:18])=[O:17])[O:4]1)[CH3:2].[CH3:20][C:21]([S@:24]([NH2:26])=[O:25])([CH3:23])[CH3:22].[BH4-].[Na+]>C1COCC1.[O-]CC.[Ti+4].[O-]CC.[O-]CC.[O-]CC>[CH2:1]([CH:3]1[CH2:9][CH:8]([NH:26][S:24]([C:21]([CH3:23])([CH3:22])[CH3:20])=[O:25])[CH2:7][CH2:6][CH:5]([C:11]2[N:12]([CH3:19])[N:13]=[CH:14][C:15]=2[N+:16]([O-:18])=[O:17])[O:4]1)[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 4311764Sodium borohydrideHCID 10964479tert-Butylsulfinamide, (R)-(+)-HCID 867137802-Ethyl-7-(2-methyl-4-nitro-pyrazol-3-yl)oxepan-4-one

生成物 1

HCID 86713781N-(2-ethyl-7-(2-methyl-4-nitro-pyrazol-3-yl)oxepan-4-yl)-2-methyl-propane-2-sulfinamide

試薬・触媒・溶媒 2

HCID 76524Titanium tetraethoxide触媒
HCID 8028
Tetrahydrofuran
溶媒
2 回

実験手順

To a solution of 2-ethyl-7-(2-methyl-4-nitro-pyrazol-3-yl)oxepan-4-one (120 mg, 0.45 mmol) in THF (3 mL) was added (R)-2-methylpropane-2-sulfinamide (70 mg, 0.58 mmol) followed by titanium(IV) ethoxide (0.30 mL, 1.12 mmol). The reaction mixture was heated at reflux for 4 hr then allowed to cool to room temperature. The crude solution was added dropwise to a solution of sodium borohydride (69 mg, 1.80 mmol) in THF (3 mL) at −60° C. The reaction mixture was warmed to 0° C., quenched with MeOH (3 mL) and brine (50 mL), and stirred at room temperature for 18 hr. The mixture was filtered through Celite® washing with EtOAc (200 mL). The aqueous layer was extracted with EtOAc (3×50 mL) and the combined organic layers were washed with brine (150 mL), separated, dried over MgSO4 and concentrated under reduced pressure. Purification via silica gel column chromatography (0-10% MeOH/DCM) gave N-(2-ethyl-7-(2-methyl-4-nitro-pyrazol-3-yl)oxepan-4-yl)-2-methyl-propane-2-sulfinamide as a mixture of diastereomers (ratio 5:2) as a colourless solid (118 mg, 71% over two steps). 1H NMR (400 MHz, CDCl3) δ 8.03 and 8.02 (2s, 1H), 5.60-5.51 (m, 1H), 4.08 and 4.06 (2s, 3H), 3.83-3.66 (m, 2H), 3.62-3.50 (m, 1H), 3.22 and 3.15 (d, J=6.2 and 4.0 Hz, 1H), 2.11-1.96 (m, 4H), 1.76 (s, 1H), 1.63-1.54 (m, 2H), 1.28-1.15 (m, 9H), 0.91 (td, J=7.4, 2.4 Hz, 3H).

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 4 hr
  3. temperatureThe reaction mixture was warmed to 0° C.
  4. customquenched with MeOH (3 mL) and brine (50 mL)
  5. filtrationThe mixture was filtered through Celite®
  6. washwashing with EtOAc (200 mL)
  7. extractionThe aqueous layer was extracted with EtOAc (3×50 mL)
  8. washthe combined organic layers were washed with brine (150 mL)
  9. customseparated
  10. dry with materialdried over MgSO4
  11. concentrationconcentrated under reduced pressure
  12. customPurification via silica gel column chromatography (0-10% MeOH/DCM)

出典と根拠

ORDレコード
ord-f954f041c51a410cac00ea1a3515fc4a
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09328106B2

反応ノート

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