Diisopropylethylamine → HCID 67099598, 화합물
반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]1([CH2:15][CH2:14][CH2:13][CH2:12]1)[C:7](=[O:16])[C:6]([C:17](OCC)=[O:18])=[C:5]2[OH:22].Cl.[C:24]([O:28][C:29](=[O:32])[CH2:30][NH2:31])([CH3:27])([CH3:26])[CH3:25].CCN(C(C)C)C(C)C>O1CCOCC1>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]1([CH2:12][CH2:13][CH2:14][CH2:15]1)[C:7](=[O:16])[C:6]([C:17]([NH:31][CH2:30][C:29]([O:28][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:32])=[O:18])=[C:5]2[OH:22]참가 물질
5
반응 조건
- 온도
- 85 °C
실험 절차
A mixture of ethyl 6′-chloro-4′-hydroxy-2′-oxo-spiro[cyclopentane-1,1′-naphthalen]-3′-carboxylate (0.66 g, 2 mmol) and glycine tert-butyl ester hydrochloride (0.5 g, 3 mmol) in 10 mL dioxane was treated with DIPEA (1 mL, 6 mmol). The mixture was warmed to 85° C. and stirred for 4 hours, M+1=406. The mixture was then cooled to room temperature and concentrated in vacuo. The crude product was purified by column chromatography eluting with 10-30% EtOAc hexane to give the title compound (0.8 g) as a pale yellow solid. MS (m/z)=406 (M+Na)+.
후처리
- temperatureThe mixture was then cooled to room temperature
- concentrationconcentrated in vacuo
- customThe crude product was purified by column chromatography
- washeluting with 10-30% EtOAc hexane
출처 및 근거
- ORD 기록
- ord-71524097648e428ca23593cd69b2e84b
- 출처 데이터셋
- uspto-grants-2009_12
- 특허 번호
- US07635715B2
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