반응식
[F-:1].[K+].C1N2CCOCCOCCN(CCOCCOCC2)CCOCCOC1.Cl[CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=1[S:37][CH2:38][CH2:39][CH:40]1[O:44][CH2:43][CH2:42][O:41]1>C(#N)C>[F:1][CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=1[S:37][CH2:38][CH2:39][CH:40]1[O:44][CH2:43][CH2:42][O:41]1참가 물질
실험 절차
Potassium fluoride (3.5 mg, 0.060 mmol) and kryptofix 222 (22.5 mg, 0.060 mmol) were dissolved in acetonitrile (1 ml) and added to 2-[2-(2-chloromethyl-phenylsulfanyl)-ethyl]-[1,3]dioxolane (7.7 mg, 0.030 mmol) in acetonitrile (1 ml). The reaction mixture was heated to 70 degrees for 30 minutes. The crude product was purified by reverse phase preparative chromatography (Vydac 218TP1022 column; solvents A=water/0.1% TFA and B=CH3CN/0.1% TFA; gradient 40-80% B over 40 min; flow 10 ml/minute; detection at 254 nm). The fractions were left in the fridge overnight and to the acetonitrile phase was added diethyl ether, dried (Na2SO4) and evaporated under reduced pressure. (Analytical HPLC: Vydac 218TP54 column; solvents: A=water/0.1% TFA and B=CH3CN/0.1% TFA; gradient 40-80% B over 20 min; flow 1.0 ml/minute; retention time 9.200 minutes detected at 214 and 254 nm). Structure verified by NMR.
후처리
- temperatureThe reaction mixture was heated to 70 degrees for 30 minutes
- customThe crude product was purified by reverse phase preparative chromatography (Vydac 218TP1022 column; solvents A=water/0.1% TFA and B=CH3CN/0.1% TFA; gradient 40-80% B over 40 min; flow 10 ml/minute; detection at 254 nm)
- additionwas added diethyl ether
- dry with materialdried (Na2SO4)
- customevaporated under reduced pressure
- waitgradient 40-80% B over 20 min
출처 및 근거
- ORD 기록
- ord-35735f1d33d54c8ab1e2ca5bd46efe7c
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08197793B2
연결된 노트
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