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Water → tert-Butyl 4-((1S)-1-{[(benzyloxy)carbonyl]amino}ethyl)benzoate

HRID 1293179
ノート
印刷プレビュー

反応式

HRID 1293179 の反応式
[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:14]1[CH:22]=[CH:21][C:17]([C:18]([OH:20])=[O:19])=[CH:16][CH:15]=1)[CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[C:30]([CH3:33])([CH3:32])[CH3:31].O>[Cl-].C([N+](CC)(CC)CC)C1C=CC=CC=1.CN(C)C(=O)C>[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:14]1[CH:15]=[CH:16][C:17]([C:18]([O:20][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:19])=[CH:21][CH:22]=1)[CH3:13])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=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

7

反応物 4

HCID 962WaterHCID 10485t-Butyl bromideHCID 11430Potassium CarbonateHCID 575722614-[(1S)-1-[[(Benzyloxy)carbonyl]amino]ethyl]benzoic acid

生成物 1

HCID 69048022tert-Butyl 4-((1S)-1-{[(benzyloxy)carbonyl]amino}ethyl)benzoate収率 79%

試薬・触媒・溶媒 2

HCID 66133
Benzyl triethylammonium chloride
触媒
HCID 31374Dimethylacetamide溶媒

反応条件

温度
55 °C

実験手順

To a solution of 4-((1S)-1-{[(benzyloxy)carbonyl]amino}ethyl)benzoic acid (step 1, 3.7 g, 12.4 mmol) and benzyltriethylammonium chloride (3.0 g, 13 mmol) in N,N-dimethylacetamide (100 mL) was added anhydrous potassium carbonate (47 g, 340 mmol) followed by 2-bromo-2-methylpropane (89 g, 650 mmol). The resulting mixture stirred for 24 h at 55° C. After cooling to room temperature, the reaction mixture was poured into cold water (500 mL) under stirring. The resulting solution was extracted with ethyl acetate (500 mL). The organic phase was washed with water (300 mL) and brine (200 mL), dried (sodium sulfate), and evaporated. The residue was purified by flush column chromatography on silica gel (150 g) eluting with hexane/ethyl acetate (3/1) to afford 3.48 g (79%) of the title compounds as white solids: 1H-NMR (CDCl3) δ 7.95 (2H, d, J=8.3 Hz), 7.44–7.24 (7H, m), 5.15–4.99 (3H, m), 4.88 (1H, br.s), 1.58 (9H, s), 1.47 (3H, d, J=7.0 Hz).

後処理

  1. temperatureAfter cooling to room temperature
  2. stirringunder stirring
  3. extractionThe resulting solution was extracted with ethyl acetate (500 mL)
  4. washThe organic phase was washed with water (300 mL) and brine (200 mL)
  5. dry with materialdried (sodium sulfate)
  6. customevaporated
  7. customThe residue was purified
  8. customby flush column chromatography on silica gel (150 g)
  9. washeluting with hexane/ethyl acetate (3/1)

出典と根拠

ORDレコード
ord-6e9ca82eae894ac081175c7c47b05da5
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07238714B2

反応ノート

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