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【结 构 式】

【分子编号】66841

【品名】tert-butyl 2-(tert-butylamino)acetate

【CA登记号】 

【 分 子 式 】C10H21NO2

【 分 子 量 】187.28228

【元素组成】C 64.13% H 11.3% N 7.48% O 17.09%

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:(III)

 

1 Krishnan L, Sum PE, Daigneault S, et aL. 2006. Process for the prepantion of tigecycline and methods of preparing 9-aminominocycline. W0 2006130500
2 Krishnan L, Sum PE, Daigneault S, et al. 2006. Preparation of tigecycline and 9-nitrominocycline. W0 2006130501
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IX) 66846 (4S,4aS,5aR,12aS)-9-amino-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-2-naphthacenecarboxamide hydrochloride   C23H28N4O7.HCl 详情 详情
(I) 17895 2-Amino-2-methylpropane; tert-butylamine; 2-methyl-2-propanamine 75-64-9 C4H11N 详情 详情
(II) 17430 2-Bromoacetic acid tert-butyl ester; tert-butyl 2-bromoacetate; tert-Butyl bromoacetate 5292-43-3 C6H11BrO2 详情 详情
(III) 66841 tert-butyl 2-(tert-butylamino)acetate   C10H21NO2 详情 详情
(IV) 66842 2-(tert-butylamino)acetic acid hydrochloride   C6H13NO2.HCl 详情 详情
(V) 66843 2-(tert-butylamino)acetyl chloride hydrochloride   C6H12ClNO.HCl 详情 详情
(VI) 65813 Minocycline hydrochloride; [4S-(4alpha,4aalpha,5aalpha,12aalpha)]-4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxonaphthacene-2-carboxamide monohydrochloride 13614-98-7 C23H27N3O7.HCl 详情 详情
(VII) 66844 (4S,4aS,5aR,12aS)-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-9-nitro-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-2-naphthacenecarboxamide monosulfate   C23H26N4O9.2H2SO4 详情 详情
(VIII) 66845 (4S,4aS,5aR,12aS)-9-amino-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-2-naphthacenecarboxamide monosulfate   C23H28N4O7.2H2SO4 详情 详情
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