4-Penten-1-OL → 3-Methyl-N-{[(pent-4-en-1-yl)oxy]carbonyl}-L-valine

HRID 388220

反応式

HRID 388220 の反応式
C(N(C(C)C)CC)(C)C.[CH2:10]([OH:15])[CH2:11][CH2:12][CH:13]=[CH2:14].Cl[C:17](Cl)([O:19]C(=O)OC(Cl)(Cl)Cl)Cl.[OH-].[Na+].[NH2:30][C@H:31]([C:36]([OH:38])=[O:37])[C:32]([CH3:35])([CH3:34])[CH3:33]>O1CCOCC1>[CH3:33][C:32]([CH3:35])([CH3:34])[C@H:31]([NH:30][C:17]([O:15][CH2:10][CH2:11][CH2:12][CH:13]=[CH2:14])=[O:19])[C:36]([OH:38])=[O:37]

参加物

7

反応条件

温度
0 °C

実験手順

Diisopropylethyl amine (9.85 g, 76.2 mmol) was added dropwise to a 0° C. solution of 4-penten-1-ol (7.22 g, 83.9 mmol) and triphosgene (11.3 g, 38.1 mmol) in 160 mL dioxane. The resulting white suspension was stirred for 5 minutes at 0° C., then allowed to warm to 25° C. over 1 hour. The suspension was cooled to 0° C. with an ice bath and 1 N NaOH (76.2 mL) and L-t-butylglycine (10.0 g, 76.2 mmol) were added. The reaction mixture was warmed to 25° C. and stirred for 18 hours. The dioxane was removed in vacuo and the reaction mixture was basified to pH 12 with 1 N NaOH. The aqueous layer was extracted with DCM (3×150 mL), then acidified to pH˜1 with 6 N HCl. The aqueous layer was extracted with DCM (3×150 mL). The combined organic layers were dried over MgSO4 and concentrated to give the compound as a tan oil (13.7 g, 73.9% yield). LRMS (ESI) m/z 244 [(M+H)+; calcd for C12H22NO4 244].

後処理

  1. temperatureto warm to 25° C. over 1 hour
  2. temperatureThe suspension was cooled to 0° C. with an ice bath
  3. temperatureThe reaction mixture was warmed to 25° C.
  4. stirringstirred for 18 hours
  5. customThe dioxane was removed in vacuo
  6. extractionThe aqueous layer was extracted with DCM (3×150 mL)
  7. extractionThe aqueous layer was extracted with DCM (3×150 mL)
  8. dry with materialThe combined organic layers were dried over MgSO4
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-b6397d4c317d4728ba5e258f4cfa1ffb
出典データセット
uspto-grants-2013_02
特許番号
US08377873B2

関連ノート

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