5,6-Dimethoxyisoindoline → HCID 49850118, 화합물
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C(OC1C=CC=CC=1CN(CC1C=CC=CN=1)CCCCCCC1CCC(C2C=CC=CC=2OC)CC1)(C)(C)C.Br[CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][N:48]([CH2:56][C:57]1[CH:62]=[CH:61][CH:60]=[CH:59][C:58]=1[O:63][C:64]([CH3:67])([CH3:66])[CH3:65])[CH2:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][N:51]=1.[CH3:68][O:69][C:70]1[CH:71]=[C:72]2[C:76](=[CH:77][C:78]=1[O:79][CH3:80])[CH2:75][NH:74][CH2:73]2>>[C:64]([O:63][C:58]1[CH:59]=[CH:60][CH:61]=[CH:62][C:57]=1[CH2:56][N:48]([CH2:49][C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][N:51]=1)[CH2:47][CH2:46][CH2:45][CH2:44][CH2:43][CH2:42][N:74]1[CH2:75][C:76]2[C:72](=[CH:71][C:70]([O:69][CH3:68])=[C:78]([O:79][CH3:80])[CH:77]=2)[CH2:73]1)([CH3:67])([CH3:66])[CH3:65]참가 물질
4
실험 절차
The same procedure as described for compound 11 was applied to starting material 10 (0.428 g, 0.988 mmol) and 5,6-dimethoxyisoindoline (0.175 g, 0.975 mmol). Purification was carried out on a silica gel TLC plate that was developed in with a 5% methanolic NH3 (7 M NH3 in methanol/95% CH2Cl2. The product was isolated as pale yellow oil (60%). 1H NMR (CDCl3) δ 8.446 (dd, 1H, Ar), 7.72 (m, 3H, Ar), 7.062 (m, 2H, Ar), 6.981 (ddd, 2H, Ar), 6.888 (s, 2H, Ar), 3.816 (s, 4H, —CH2—CH2—), 3.792 (s, 6H, —OCH3—), 3.714 (s, 2H, —CH2—), 3.637 (s, 2H, —CH2—), 2.611 (t, 2H, —CH2—), 2.436 (t, 2H, —CH2—), 1.503 (m, 4H, —CH2—CH2—), 1.319 (s, 9H, —C(CH3)3), 1.275 (m, 4H, —CH2—CH2—). Mass Spec.=531.73 (M+H)+.
후처리
- customPurification
출처 및 근거
- ORD 기록
- ord-91d53d2c45b04d5090601db44dcff3a7
- 출처 데이터셋
- uspto-grants-2014_06
- 특허 번호
- US08747810B2
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