반응식
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]참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
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].
후처리
- temperatureto warm to 25° C. over 1 hour
- temperatureThe suspension was cooled to 0° C. with an ice bath
- temperatureThe reaction mixture was warmed to 25° C.
- stirringstirred for 18 hours
- customThe dioxane was removed in vacuo
- extractionThe aqueous layer was extracted with DCM (3×150 mL)
- extractionThe aqueous layer was extracted with DCM (3×150 mL)
- dry with materialThe combined organic layers were dried over MgSO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-b6397d4c317d4728ba5e258f4cfa1ffb
- 출처 데이터셋
- uspto-grants-2013_02
- 특허 번호
- US08377873B2
연결된 노트
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