Hydrochloric Acid → HCID 59843201、化合物

HRID 2196497

反応式

HRID 2196497 の反応式
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH3:20])[C:10]([O:12]N1C(=O)CCC1=O)=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[O:21]1[CH:25]=[CH:24][CH:23]=[C:22]1[C:26]1[N:30]([C:31]2[CH:32]=[C:33]([CH2:36][NH2:37])[S:34][CH:35]=2)[N:29]=[C:28]([C:38]([F:41])([F:40])[F:39])[CH:27]=1.CCN(CC)CC.Cl>C(Cl)Cl.CN(C=O)C>[O:21]1[CH:25]=[CH:24][CH:23]=[C:22]1[C:26]1[N:30]([C:31]2[CH:32]=[C:33]([CH2:36][NH:37][C:10](=[O:12])[C@@H:9]([NH:8][C:6](=[O:7])[O:5][C:1]([CH3:2])([CH3:3])[CH3:4])[CH3:20])[S:34][CH:35]=2)[N:29]=[C:28]([C:38]([F:40])([F:41])[F:39])[CH:27]=1

参加物

7

実験手順

(S)-2,5-Dioxopyrrolidin-1-yl 2-(tert-butoxycarbonylamino)propanoate (130 mg, 0.45 mmol) was added to amine 5 (110 mg, 0.35 mmol) and Et3N (94.4 mg, 130 μL, 0.93 mmol) in DCM (2 mL) and DMF (0.2 mL) and the mixture was stirred at room temperature for 36 h. DCM was added followed by 1N HCl and the organic layer was separated and washed with H2O, then with saturated NaHCO3, dried over MgSO4, filtered and concentrated. The crude material was purified by chromatography (Biotage, 25+S column) eluting with 0-50% EtOAc/hexanes. Compound 6 was obtained in 49% yield as a white solid. LRMS (ESI): calc. 484.5; found 507.1 (MNa)+.

後処理

  1. customthe organic layer was separated
  2. washwashed with H2O
  3. dry with materialwith saturated NaHCO3, dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude material was purified by chromatography (Biotage, 25+S column)
  7. washeluting with 0-50% EtOAc/hexanes

出典と根拠

ORDレコード
ord-7324f87f93a8403c9c040e9e6e16a035
出典データセット
uspto-grants-2012_12
特許番号
US08338437B2

関連ノート

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