Methanol → 2-(4-Nitrobenzyl)-1,4,7,10,13,16-hexaazacyclooctadecane
반응식
[N+:1]([C:4]1[CH:30]=[CH:29][C:7]([CH2:8][CH:9]2[NH:26][CH2:25][C:24](=O)[NH:23][CH2:22][CH2:21][NH:20][CH2:19][CH2:18][NH:17][CH2:16][CH2:15][NH:14][CH2:13][CH2:12][NH:11][C:10]2=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].CO>C1COCC1.O>[N+:1]([C:4]1[CH:30]=[CH:29][C:7]([CH2:8][CH:9]2[CH2:10][NH:11][CH2:12][CH2:13][NH:14][CH2:15][CH2:16][NH:17][CH2:18][CH2:19][NH:20][CH2:21][CH2:22][NH:23][CH2:24][CH2:25][NH:26]2)=[CH:6][CH:5]=1)([O-:3])=[O:2]참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
A solution of BH3 in THF (100 mmol) was added dropwise to a stirred suspension of 3-(4-nitrobenzyl)-2,6-dioxo-1,4,7,10,13,16-hexaazacyclooctadecane (4) (10 mmol) in THF (50 ml) at 0° C. under nitrogen atmosphere. The solution was heated at reflux for 36 hours. Methanol was added slowly to the solution at 0° C. after which the solvent was removed and the residue was dissolved in methanol (50 ml); the resulting mixture was cooled at 0° C. and gaseous HCl was bubbled through the solution and then the mixture was refluxed for 12 hours. The resulting precipitate was collected washed with ether to give a white powder. The solid was dissolved in water and was loaded on a column of DOWEX 1X-8 anion-exchange resin (OH− form). The column was eluted with water; alkaline fractions were collected, and the water was removed under vacuum to give pale yellow oil. The yield was 55%.
후처리
- temperatureThe solution was heated
- temperatureat reflux for 36 hours
- customwas removed
- dissolutionthe residue was dissolved in methanol (50 ml)
- customgaseous HCl was bubbled through the solution
- temperaturethe mixture was refluxed for 12 hours
- customThe resulting precipitate was collected
- washwashed with ether
- customto give a white powder
- washThe column was eluted with water
- customalkaline fractions were collected
- customthe water was removed under vacuum
- customto give pale yellow oil
출처 및 근거
- ORD 기록
- ord-bc29a12cb048463e89f1fc5759d52d43
- 출처 데이터셋
- uspto-grants-2006_11
- 특허 번호
- US07132513B2
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