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【结 构 式】

【分子编号】66165

【品名】sodium (6S,7S)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

【CA登记号】 

【 分 子 式 】C14H14NaN5O6S2

【 分 子 量 】435.417

【元素组成】C 38.625 H 3.24% Na 5.28% N 16.08% O 22.05% S 14.73%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(I)

1 撒应福,任秉钧.2006.头孢类抗生素的制备方法,发明专利申请公开说明书.CN 1763046
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) 66165 sodium (6S,7S)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate   C14H14NaN5O6S2 详情 详情
(II) 11159 iodomethyl pivalate C6H11IO2 详情 详情
(III) 66166 (6R,7R)-tert-butoxymethyl 7-((E)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate   C19H25N5O7S2 详情 详情
(IV) 66167 (6S,7S)-tert-butoxymethyl 7-((E)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate   C19H24ClN5O6S2 详情 详情
(V) 66168 (6R,7R)-tert-butoxymethyl 7-((E)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(iodomethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate   C19H24IN5O6S2 详情 详情
(VI) 66169 (((6S,7S)-7-((E)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-2-((tert-butoxymethoxy)carbonyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)triphenylphosphonium iodide   C37H39IN5O6S2P 详情 详情
(VII) 66170 (6R,7R)-tert-butoxymethyl 7-((E)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-8-oxo-3-((triphenylphosphoranylidene)methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate, iodide salt   C37H38N5O6S2P 详情 详情
(VIII) 11153 4-Methyl-1,3-thiazole-5-carbaldehyde 82294-70-0 C5H5NOS 详情 详情
Extended Information