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【结 构 式】

【分子编号】51624

【品名】(2R,3S,4R,5S)-2-(hydroxymethyl)-3,4,5-piperidinetriol

【CA登记号】

【 分 子 式 】C6H13NO4

【 分 子 量 】163.17356

【元素组成】C 44.17% H 8.03% N 8.58% O 39.22%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(I)

The title compound was synthesized by reductive alkylation of deoxygalactojirimycin (I) with nonylaldehyde (II) in the presence of sodium cyanoborohydride.

1 Jacob, G.S.; Butters, T.D.; Fleet, G.W.J.; Carrouee, S.; Dwek, R.A.; Platt, F.M.; Zitzmann, N.; Picker, D.H.; Long chain N-alkyl cpds. and oxa-derivs. thereof. WO 0110429 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 51624 (2R,3S,4R,5S)-2-(hydroxymethyl)-3,4,5-piperidinetriol C6H13NO4 详情 详情
(II) 38863 nonanal 124-19-6 C9H18O 详情 详情

合成路线2

该中间体在本合成路线中的序号:(I)

The title compound is prepared by reductive alkylation of deoxygalactonojirimycin (I) with butyraldehyde (II) under catalytic hydrogenation conditions in the presence of palladium black and sodium acetate buffer

1 Platt, F.M.; Neises, G.R.; Dwek, R.A.; Butters, T.D. (Pharmacia Corp.); Novel deoxygalactonojirimycin derivs.. EP 0698012; JP 1996510244; US 5399567; US 6291657; WO 9426714 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 51624 (2R,3S,4R,5S)-2-(hydroxymethyl)-3,4,5-piperidinetriol C6H13NO4 详情 详情
(II) 23694 butyraldehyde 123-72-8 C4H8O 详情 详情
Extended Information