반응식
[F:1][C:2]1[CH:29]=[CH:28][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16]N4C(O)C5C(=CC=CC=5)C4=O)[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1.C[N:31]=[C:32]=[O:33].[C:34]([O-])([O-])=O.[K+].[K+].C1C[O:43][CH2:42][CH2:41]1>>[C:32](=[O:33])([O:43][CH2:42][CH2:41][C@H:16]([CH3:34])[CH2:15][N:12]1[CH2:11][CH2:10][CH:9]([C:6]2[C:5]3[CH:28]=[CH:29][C:2]([F:1])=[CH:3][C:4]=3[O:8][N:7]=2)[CH2:14][CH2:13]1)[NH2:31]참가 물질
반응물 4
생성물 1
실험 절차
To a solution of 2-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2,3-dihydro-3-hydroxy-1H-isoindol-1-one (3.1 g, 10.6 mmol) in dry THF (120 ml) was added methyl isocyanate (0.66 ml, 11.1 mmol) followed by milled K2CO3 (2.2 g, 15.9 mmol) at room temperature, under nitrogen. The reaction mixture was stirred for 3 days at which time it was filtered through a pad of Celite and the solids washed with EtOAc. The combined filtrates were concentrated to give the crude product which was purified via flash column chromatography (silica gel, 2% Et3N/EtOAc). The product containing fractions were concentrated to give 2.7 g (73%) of the desired product as an oil which solidified on standing. Recrystallization from EtOAc/pet.ether gave the product as a solid, m.p.=72°-74° C.
후처리
- filtrationwas filtered through a pad of Celite
- washthe solids washed with EtOAc
- concentrationThe combined filtrates were concentrated
- customto give the crude product which
- customwas purified via flash column chromatography (silica gel, 2% Et3N/EtOAc)
- additionThe product containing fractions
- concentrationwere concentrated
출처 및 근거
- ORD 기록
- ord-fa4dde3795264052b7678d224a8ac443
- 출처 데이터셋
- uspto-grants-1997_01
- 특허 번호
- US05597842
연결된 노트
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