반응식
[OH:1][C@@H:2]1[CH2:20][CH2:19][C@@:18]2([CH3:21])[C@H:4]([CH2:5][CH2:6][C@@H:7]3[C:17]2=[CH:16][CH2:15][C@@:14]2([CH3:22])[C@H:8]3[CH2:9][CH2:10]/[C:11]/2=[CH:12]/[CH3:13])[CH2:3]1.C(N(CC)CC)C.[C:30](OC(=O)C)(=[O:32])[CH3:31]>C(Cl)Cl.CN(C1C=CN=CC=1)C>[C:30]([O:1][C@@H:2]1[CH2:20][CH2:19][C@@:18]2([CH3:21])[C@H:4]([CH2:5][CH2:6][C@@H:7]3[C:17]2=[CH:16][CH2:15][C@@:14]2([CH3:22])[C@H:8]3[CH2:9][CH2:10]/[C:11]/2=[CH:12]/[CH3:13])[CH2:3]1)(=[O:32])[CH3:31]참가 물질
반응물 3
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 25 °C
실험 절차
Compound 1.5 (19.0 g, 63 mmol) was dissolved in CH2Cl2 (380 mL). Triethylamine (17.6 mL, 126.6 mmol), DMAP (0.772 g, 6 mmol) and acetic anhydride (8.98 mL, 94 mmol) were added sequentially at 25° C. under a nitrogen atmosphere. The resulting solution was stirred for 2 h at 25° C., at which point the reaction was determined by TLC to be complete. The reaction was quenched by the addition of ice-water (100 mL) and the phases were separated. The aqueous layer was extracted three times with DCM (3×150 mL). The organic fractions were combined and washed with saturated brine solution (100 mL), dried over anhydrous Na2SO4 (50 g), and filtered. The filtrate was concentrated under vacuum to afford compound 1.6a (22.0 g, 95% yield) as an off-white solid.
후처리
- customThe reaction was quenched by the addition of ice-water (100 mL)
- customthe phases were separated
- extractionThe aqueous layer was extracted three times with DCM (3×150 mL)
- washwashed with saturated brine solution (100 mL)
- dry with materialdried over anhydrous Na2SO4 (50 g)
- filtrationfiltered
- concentrationThe filtrate was concentrated under vacuum
출처 및 근거
- ORD 기록
- ord-da7d24e50de54b24b7fe7918c9ca080e
- 출처 데이터셋
- uspto-grants-2013_02
- 특허 번호
- US08367852B2
연결된 노트
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