반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[I:20]I.N1C=CN=C1.[CH2:27]([O:34][C:35](=[O:48])[CH2:36][C@H:37]([NH:40][C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])[CH2:38]O)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>C(Cl)Cl>[CH2:27]([O:34][C:35](=[O:48])[CH2:36][C@H:37]([NH:40][C:41]([O:43][C:44]([CH3:47])([CH3:46])[CH3:45])=[O:42])[CH2:38][I:20])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1참가 물질
실험 절차
A suspension of polymer bound triphenyl phosphine (18.25 g, 54.76 mmol) in DCM (100 ml) is treated with iodine (12.2 g, 48.1 mmol) and the reaction mixture stirred at ambient temperature for 15 minutes. Imidazole (3.72 g, 54.7 mmol) is added and the reaction mixture stirred for a further 15 minutes. A solution of (S)-3-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester (6.76 g, 21.9 mmol) in DCM (100 ml) is added. The suspension is stirred at reflux for 1.5 hours, then filtered through Celite™ filter material, washing through with DCM. The combined organic phase is washed with an aqueous solution of 10% sodium thiosulphate, water and brine, then dried over magnesium sulphate and evaporated. The crude product is chromatographed over flash silica using 8% ethylacetate in iso-hexane as eluent to afford (S)-3-tert-butoxycarbonylamino-4-iodo-butyric acid benzyl ester. [M-BOC] 320.12
후처리
- additionA suspension of polymer
- stirringthe reaction mixture stirred for a further 15 minutes
- stirringThe suspension is stirred
- temperatureat reflux for 1.5 hours
- filtrationfiltered through Celite™
- filtrationfilter material
- washwashing through with DCM
- washThe combined organic phase is washed with an aqueous solution of 10% sodium thiosulphate, water and brine
- dry with materialdried over magnesium sulphate
- customevaporated
- customThe crude product is chromatographed over flash silica using 8% ethylacetate in iso-hexane as eluent
출처 및 근거
- ORD 기록
- ord-03e7a4abcdd845eca11b0eb3e0bc38af
- 출처 데이터셋
- uspto-grants-2007_10
- 특허 번호
- US07288537B2
연결된 노트
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