Triethylamine → 3-[2-((R)-sec-Butylamino)-3,4-dioxo-cyclobut-1-enylamino]-6-chloro-N-ethyl-2-hydroxy-N-methoxy-benzenesulfonamide

HRID 1669602ノート

反応式

HRID 1669602 の反応式
[Cl:1][C:2]1[C:7]([S:8]([N:11]([O:14][CH3:15])[CH2:12][CH3:13])(=[O:10])=[O:9])=[C:6]([OH:16])[C:5]([NH:17][C:18]2[C:21](=O)[C:20](=[O:23])[C:19]=2[O:24]CC)=[CH:4][CH:3]=1.[NH2:27][C@@H:28]([CH2:30][CH3:31])[CH3:29].C(N(CC)CC)C>CC#N.CCO>[C@H:28]([NH:27][C:21]1[C:20](=[O:23])[C:19](=[O:24])[C:18]=1[NH:17][C:5]1[C:6]([OH:16])=[C:7]([S:8]([N:11]([CH2:12][CH3:13])[O:14][CH3:15])(=[O:10])=[O:9])[C:2]([Cl:1])=[CH:3][CH:4]=1)([CH2:30][CH3:31])[CH3:29]

参加物

6

反応条件

温度
70 °C

実験手順

To a stirred solution of 6-Chloro-3-(2-ethoxy-3,4-dioxo-cyclobut-1-enylamino)-2-hydroxy-N-methoxy-N-ethyl-benzenesulfonamide (Intermediate FA) (100 mg, 0.25 mmol) in MeCN (1 ml) and EtOH (1 ml) was added (R)-(−)-2-Aminobutane (30.7 mg, 0.42 mmol) followed by triethylamine (69 μl, 0.49 mmol). The reaction mixture was heated at 70° C. for 1 hour. The reaction mixture was concentrated in vacuo and dissolved in EtOAc. The EtOAc solution was washed with 1M HCl (aq) and concentrated in vacuo. The residue was triturated with DCM to give a white solid; [M+H]+ 432.2. 1H NMR (DMSO) 0.9 (3H, t, CH3), 1.2 (6H, m), 1.5-1.6 (2H, m), 3.3 (2H, m), 3.7 (3H, s, CH3) 4.1 (1H, m), 7.3 (1H, d), 8.1 (1H, d), 8.3 (1H, d), 9.4 (1H, s), 10.1 (1H, s).

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. dissolutiondissolved in EtOAc
  3. washThe EtOAc solution was washed with 1M HCl (aq)
  4. concentrationconcentrated in vacuo
  5. customThe residue was triturated with DCM
  6. customto give a white solid

出典と根拠

ORDレコード
ord-94004b851df4424eb5f21dd651ae8d16
出典データセット
uspto-grants-2011_08
特許番号
US07989497B2

反応ノート

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