반응식
Cl.CN(C)CCCN=C=NCC.[CH:13]1[CH:14]=[CH:15][C:16]2N(O)N=N[C:17]=2[CH:18]=1.C(N(CC)CC)C.[NH2:30][CH:31]1[CH2:36][CH2:35][CH2:34][N:33]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])[CH2:32]1.CN([CH:47]=[O:48])C>>[C:47]([NH:30][CH:31]1[CH2:36][CH2:35][CH2:34][N:33]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])[CH2:32]1)(=[O:48])[C:17]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:18]=1참가 물질
6
실험 절차
A solution of benzoic add (0.123 g) in DMF (5 ml) was treated with 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.231 g), HOBT (0.163 g) and triethylamine (0.56 ml) and stirred at room temperature for 1 h. A solution of 3-amino-1-N-Boc-piperidine (0.3 g) in DMF (1 ml) was then added and stirring continued for 18 h. The solution was concentrated under reduced pressure to give an oil which was partitioned between ethyl acetate and water. The separated organic extracts were washed with water, hydrochloric acid (2N), saturated sodium bicarbonate solution and brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give the title compound (0.120 g) as a yellow solid.
후처리
- stirringstirring
- waitcontinued for 18 h
- concentrationThe solution was concentrated under reduced pressure
- customto give an oil which
- customwas partitioned between ethyl acetate and water
- washThe separated organic extracts were washed with water, hydrochloric acid (2N), saturated sodium bicarbonate solution and brine
- dry with materialdried (over magnesium sulphate)
- concentrationconcentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-e1e715609e01411ba597fa73de2bd029
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07084139B2
연결된 노트
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