Diisopropylethylamine → (1R)-1'-({1-[4-(Pyridin-4-ylmethoxy)phenyl]cyclopropyl}-carbonyl)-3H-spiro[2-benzofuran-1,3'-pyrrolidin]-3-one
반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([C:11]([OH:13])=O)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[NH:14]1[CH2:18][CH2:17][C@@:16]2([C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=3[C:20](=[O:27])[O:19]2)[CH2:15]1.[CH3:28][C:29]1(C)[C@@H]2CC[C@@:30]1([CH2:37]S(O)(=O)=O)[C:31](=O)[CH2:32]2.F[P-](F)(F)(F)(F)F.[N:50]1(O[P+](N(C)C)(N(C)C)N(C)C)C2C=CC=CC=2N=N1.C(N(CC)C(C)C)(C)C>C(Cl)Cl>[N:50]1[CH:32]=[CH:31][C:30]([CH2:37][O:1][C:2]2[CH:3]=[CH:4][C:5]([C:8]3([C:11]([N:14]4[CH2:18][CH2:17][C@@:16]5([C:22]6[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=6[C:20](=[O:27])[O:19]5)[CH2:15]4)=[O:13])[CH2:9][CH2:10]3)=[CH:6][CH:7]=2)=[CH:29][CH:28]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
A mixture of 1-(4-hydroxyphenyl)cyclopropanecarboxylic acid (0.20 g, 1.1 mmol), [(1S,4R)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulfonic acid-(1R)-3H-spiro[2-benzofuran-1,3′-pyrrolidin]-3-one salt (0.47 g, 1.1 mmol), Benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (0.55 g, 1.2 mmol), and N,N-diisopropylethylamine (0.49 ml, 2.8 mmol) in methylene chloride (3 ml) was stirred at r.t. overnight. Then the reaction was quenched with water, and the reaction mixture was extracted with ethyl acetate. The extract was washed with 1N HCl aqueous solution (x2), water and brine successively; then dried over Na2SO4; and then filtered. The filtrate was concentrated to afford the desired product (0.35 g, yield: 89%).
후처리
- customThen the reaction was quenched with water
- extractionthe reaction mixture was extracted with ethyl acetate
- washThe extract was washed with 1N HCl aqueous solution (x2), water and brine successively
- dry with materialthen dried over Na2SO4
- filtrationand then filtered
- concentrationThe filtrate was concentrated
출처 및 근거
- ORD 기록
- ord-1e7d133630fa422d98624dfb404f66cf
- 출처 데이터셋
- uspto-grants-2011_11
- 특허 번호
- US08058288B2
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