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Triethylamine → (R)-N-(2-phenylpropyl)propane-2-sulfonamide

HRID 521740
ノート
印刷プレビュー

反応式

HRID 521740 の反応式
Cl.[C:2]1([CH:8]([CH3:11])[CH2:9][NH2:10])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CCN(CC)CC.[CH3:19][CH:20]([S:22](Cl)(=[O:24])=[O:23])[CH3:21]>CN(C1C=CN=CC=1)C.C(Cl)Cl>[C:2]1([CH:8]([CH3:11])[CH2:9][NH:10][S:22]([CH:20]([CH3:21])[CH3:19])(=[O:24])=[O:23])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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 8471TriethylamineHCID 824082-Propanesulfonyl chlorideHCID 893322-Phenylpropylamine hydrochloride

生成物 1

HCID 21893415(R)-N-(2-phenylpropyl)propane-2-sulfonamide収率 86%

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6344Dichloromethane
溶媒

実験手順

To a solution of 2-phenyl-propylamine HCl salt (1.0 g, 5.8 mmol), DMAP (35 mg, 0.3 mmol) and Et3N (1.77 g, 17.5 mmol) in DCM (25 mL) was added propane-2-sulfonyl chloride (1.25 g, 8.7 mmol) dropwise at 0° C. The mixture was stirred at r.t. for 16 h, and was then concentrated under vacuum. The residue was partitioned between EtOAc (100 mL) and H2O (10 mL). The organic layer was separated and washed with brine (10 mL), dried over anhydrous Na2SO4, filtrated and concentrated to give an oil residue. This residue was purified with silica gel column (Hexane/EtOAc=2/1 to 1/1) to obtain the desired product (1.2 g, 86%) as a pale yellow oil. 1H NMR (600 MHz, CDCl3) δ 7.30-7.32 (m, 2H), 7.18-7.24 (m, 3H), 3.90-3.94 (m, 1H), 3.30-3.35 (m, 1H), 3.18-3.22 (m, 1H), 2.99-3.04 (m, 1H), 2.91-2.95 (m, 1H), 1.27 (d, 3H, J=7.2 Hz), 1.25 (d, H, J=7.8 Hz), 1.22 (d, 1H, J=7.2 Hz).

後処理

  1. concentrationwas then concentrated under vacuum
  2. customThe residue was partitioned between EtOAc (100 mL) and H2O (10 mL)
  3. customThe organic layer was separated
  4. washwashed with brine (10 mL)
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltrated
  7. concentrationconcentrated
  8. customto give an oil residue
  9. customThis residue was purified with silica gel column (Hexane/EtOAc=2/1 to 1/1)

出典と根拠

ORDレコード
ord-3b0e97b9696448e195819d4c87ec5f59
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09328125B2

反応ノート

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