7-Nitro-1,2,3,4-tetrahydroquinoline → 1-(2-Dimethylaminoacetyl)-7-nitro-1,2,3,4-tetrahydroquinoline
반응식
[N+:1]([C:4]1[CH:13]=[C:12]2[C:7]([CH2:8][CH2:9][CH2:10][NH:11]2)=[CH:6][CH:5]=1)([O-:3])=[O:2].Cl.[CH3:15][N:16]([CH2:18][C:19](Cl)=[O:20])[CH3:17]>>[CH3:15][N:16]([CH3:17])[CH2:18][C:19]([N:11]1[C:12]2[C:7](=[CH:6][CH:5]=[C:4]([N+:1]([O-:3])=[O:2])[CH:13]=2)[CH2:8][CH2:9][CH2:10]1)=[O:20]참가 물질
3
실험 절차
Using the procedure outlined in Description 4 followed by silica SPE chromatography eluting with 20% EtOAc/MeOH the title compound was prepared from 7-nitro-1,2,3,4-tetrahydroquinoline (D1) (178 mg, 1 mmol) and dimethylaminoacetyl chloride hydrochloride (174 mg, 1.1 mmol) as a yellow solid (103 mg). 1H NMR (250 MHz, CDCl3) δ (ppm): 8.74 (d, 1H), 7.92 (dd, 1H), 7.28 (d, 1H), 3.87 (m, 2H), 3.25 (s, 2H), 2.87 (t, 2H), 2.35 (s, 6H), 1.95 (m, 2H).
후처리
- washeluting with 20% EtOAc/MeOH the title compound
출처 및 근거
- ORD 기록
- ord-78ef6847a0664fde9b0aeb2bf20960be
- 출처 데이터셋
- uspto-grants-2009_05
- 특허 번호
- US07538121B2
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