Bromoacetic Acid → N-(5-Amino-1-carboxypentyl)iminodiacetic acid
반응식
Br[CH2:2][C:3]([OH:5])=[O:4].C(OC([NH:16][CH2:17][CH2:18][CH2:19][CH2:20][C@@H:21]([C:23]([OH:25])=[O:24])[NH2:22])=O)C1C=CC=CC=1>[OH-].[Na+]>[C:3]([CH2:2][N:22]([CH2:2][C:3]([OH:5])=[O:4])[C@H:21]([C:23]([OH:25])=[O:24])[CH2:20][CH2:19][CH2:18][CH2:17][NH2:16])([OH:5])=[O:4]참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
Bromacetic acid (28 g, 200 mmole) was dissolved in 100 ml of 2 M sodium hydroxide (NaOH) and cooled to 0° C. A solution of 28 g (100 mmole) of N'-benzyloxycarbonyl-L-lysine in 150 ml of 2 M NaOH was slowly added dropwise into the bromacetic acid solution while stirring in a 0° C. cooling bath. After 2 hours, the cooling bath was removed and the solution was stirred overnight at room temperature. The solution was then heated for two hours at 50° C. and 300 ml of 1 M hydrochloric acid (HCl) was added dropwise. The mixture was then cooled to room temperature allowing the N'-benzyloxycarbonyl-nitrilotriacetic acid (Z-NTA) to precipitate. The Z-NTA was collected by filtration and further purified by dissolving in 1 M NaOH, re-precipitating with the same amount of 1 M HCl and filtering. The dissolving and precipitating cycle was repeated twice.
후처리
- temperaturecooling bath
- customthe cooling bath was removed
- stirringthe solution was stirred overnight at room temperature
- temperatureThe solution was then heated for two hours at 50° C.
- addition300 ml of 1 M hydrochloric acid (HCl) was added dropwise
- temperatureThe mixture was then cooled to room temperature
- customto precipitate
- filtrationThe Z-NTA was collected by filtration
- customfurther purified
- dissolutionby dissolving in 1 M NaOH
- customre-precipitating with the same amount of 1 M HCl
- filtrationfiltering
- customThe dissolving and precipitating cycle
출처 및 근거
- ORD 기록
- ord-98f200f7ee1649548d566e7161107936
- 출처 데이터셋
- uspto-grants-2000_07
- 특허 번호
- US06087452
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