Triethylamine → HCID 54290744、化合物

反応式

[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:14]([OH:16])=O)[CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH2:18][CH2:19][P:20](=[O:25])([O:23][CH3:24])[O:21][CH3:22].C(N(CC)CC)C>CN(C)C=O>[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:14]([NH:18][CH2:19][P:20](=[O:25])([O:23][CH3:24])[O:21][CH3:22])=[O:16])[CH3:13])=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

実験手順

9.6 g (0.03 mol) of the N-hydroxysuccinimide ester of N-benzyloxycarbonyl-L-alanine and 5.26 g (0.03 mol) of dimethyl aminomethylphosphonate hydrochloride were stirred in 65 ml of dry dimethylformamide. While stirring and maintaining the temperature below 20° C, there were added dropwise 4.2 ml of dry triethylamine. The mixture was then stirred overnight at room temperature. The triethylamine hydrochloride was filtered off and washed with a little dimethylformamide. The filtrate was evaporated under an oil-pump vacuum and at a bath temperature below 40° C. The residual oil was treated with 40 ml of water and the resulting mixture extracted with four 40 ml portions of chloroform. The combined organic phases were washed with a small volume of a strong potassium carbonate solution and then dried over sodium sulphate. The sodium sulphate was filtered off and the filtrate evaporated first under a water-pump vacuum and then under an oil-pump vacuum. There were obtained 11.0 g of dimethyl [(N-benzyloxycarbonyl-L-alanyl)amino]-methylphosphonate as an oil with the expected N.M.R. spectrum.