Triethylamine → 4-[2-(1,1-Dioxo-isothiazolidin-2-yl)-ethyl]-piperazine-1-carboxylic acid tert-butyl ester
반응식
[C:1]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][NH2:16])[CH2:10][CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].C(N(CC)CC)C.Cl[CH2:25][CH2:26][CH2:27][S:28](Cl)(=[O:30])=[O:29]>C1COCC1>[C:4]([O:3][C:1]([N:8]1[CH2:9][CH2:10][N:11]([CH2:14][CH2:15][N:16]2[CH2:25][CH2:26][CH2:27][S:28]2(=[O:30])=[O:29])[CH2:12][CH2:13]1)=[O:2])([CH3:7])([CH3:6])[CH3:5]참가 물질
실험 절차
To a stirred solution of 1-Boc-4-(2-aminoethyl)-piperazine (1.26 g, 6.8 mmol) and triethylamine (1 mL) in THF (10 ML), 3-chloro-propylsulfonyl chloride (Aldrich, 0.68 mL, 6.94 mmol) was added slowly at room temperature. The mixture was stirred for 30 minutes at and the reaction was quenched with water. The new mixture was extracted with ethyl acetate and the extracts were combined and dried (Na2SO4). The solution was concentrated and the residue was dissolved in THF (20 mL) and Cs2CO3 (500 mg), NaI (80 mg) were added and the mixture was stirred at reflux overnight. The mixture was cooled to room temperature and poured into water. The new mixture was extracted with ethyl acetate (3×15 mL) and the extracts were combined and dried (Na2SO4). Removal of the solvent on a rotary evaporator gave a solid. 2.01 g.
후처리
- customwas quenched with water
- extractionThe new mixture was extracted with ethyl acetate
- dry with materialdried (Na2SO4)
- concentrationThe solution was concentrated
- dissolutionthe residue was dissolved in THF (20 mL)
- additionCs2CO3 (500 mg), NaI (80 mg) were added
- stirringthe mixture was stirred
- temperatureat reflux overnight
- additionpoured into water
- extractionThe new mixture was extracted with ethyl acetate (3×15 mL)
- dry with materialdried (Na2SO4)
- customRemoval of the solvent
- customon a rotary evaporator
- customgave a solid
출처 및 근거
- ORD 기록
- ord-1022d81cd44f481baa69582f04df677c
- 출처 데이터셋
- uspto-grants-2009_02
- 특허 번호
- US07495007B2
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