tert-Butyl Formate → HCID 68596726、化合物

HRID 270614

反応式

HRID 270614 の反応式
[C:1]([O:5][C:6]([NH:8][C@H:9]1[CH2:13][C@@:12]([C@H:18]2[CH2:22][CH2:21][O:20][CH2:19]2)([C:14]([O:16]C)=[O:15])[CH:11]=[CH:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].O.[OH-].[Li+].C(OC(C)(C)C)=O>O1CCCC1.CO.O>[C:1]([O:5][C:6]([NH:8][C@H:9]1[CH2:13][C@@:12]([C@H:18]2[CH2:22][CH2:21][O:20][CH2:19]2)([C:14]([OH:16])=[O:15])[CH:11]=[CH:10]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

参加物

7

実験手順

To a solution of methyl (1R,4S)-4-[(tert-butoxycarbonyl)amino]-1-[(3R)-tetrahydrofuran-3-yl]cyclopent-2-ene-1-carboxylate (1.60 g, 5.14 mmol) in tetrahydrofuran (27.8 mL), methanol (27.8 mL) and water (6.0 mL) was added lithium hydroxide monohydrate (0.346 g, 8.25 mmol). The pink mixture was heated to reflux for 18 h. The organic solvents were removed in vacuo and the aqueous layer was extracted once with ether and then acidified slowly with 6 M HCl until the pH reached 3-4. The resulting suspension was extracted with CH2Cl2 three times. The combined organic layers were dried over MgSO4, filtered and concentrated to give the product as a mixture of two cis/trans isomers (1.59 g) as a light yellow solid. MS calculated for C15H24NO5: (M+H) 298.2; found 198.2 (M+H-Boc).

後処理

  1. temperatureThe pink mixture was heated
  2. temperatureto reflux for 18 h
  3. customThe organic solvents were removed in vacuo
  4. extractionthe aqueous layer was extracted once with ether
  5. extractionThe resulting suspension was extracted with CH2Cl2 three times
  6. dry with materialThe combined organic layers were dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customto give the product
  10. additionas a mixture of two cis/trans isomers (1.59 g) as a light yellow solid

出典と根拠

ORDレコード
ord-b4af25f1426c499f9d89c7f7dc788b86
出典データセット
uspto-grants-2008_11
特許番号
US07449467B2

関連ノート

読み込み中…