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【结 构 式】

【分子编号】67212

【品名】benzyl (2-(methylsulfonyl)ethyl)carbamate

【CA登记号】 

【 分 子 式 】C11H15NO4S

【 分 子 量 】257.31

【元素组成】C 51.35% H 5.87% N 5.44% O 24.87% S 14.46%

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 Petrov KG, Zhang YM, Carter M, et al. 2006. Optimization and SAR for dual ErbB-1/ErbB-2 tyrosine kinase inhibition in the 6-furanylquinazoline series. Bioorganic & Medicinal Chemistry Letters, 16, 4686~4691.
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) 11240 2-(Methylsulfanyl)ethylamine; 2-(Methylthio)ethylamine; 2-(Methylsulfanyl)-1-ethanamine 18542-42-2 C3H9NS 详情 详情
(II) 67211 benzyl (2-(methylthio)ethyl)carbamate   C11H15NO2S 详情 详情
(III) 67212 benzyl (2-(methylsulfonyl)ethyl)carbamate   C11H15NO4S 详情 详情
(IV) 49880 2-(methylsulfonyl)-1-ethanamine; 2-(methylsulfonyl)ethylamine C3H9NO2S 详情 详情
(VI) 49872 1-Chloro-2-Hydroxy-5-Nitrobenzene; 2-Chloro-4-nitrophenol; 4-Nitro-2-chlorophenol; p-Nitro-o-chlorophenol 619-08-9 C6H4ClNO3 详情 详情
(VII) 17221 3-Fluorobenzyl bromide; 1-(bromomethyl)-3-fluorobenzene 456-41-7 C7H6BrF 详情 详情
(VIII) 49873 2-chloro-1-[(3-fluorobenzyl)oxy]-4-nitrobenzene; 2-chloro-4-nitrophenyl 3-fluorobenzyl ether C13H9ClFNO3 详情 详情
(IX) 49874 3-chloro-4-[(3-fluorobenzyl)oxy]phenylamine; 3-chloro-4-[(3-fluorobenzyl)oxy]aniline C13H11ClFNO 详情 详情
(X) 49875 4-chloro-6-iodoquinazoline 98556-31-1 C8H4ClIN2 详情 详情
(XI) 49876 N-[3-chloro-4-[(3-fluorobenzyl)oxy]phenyl]-N-(6-iodo-4-quinazolinyl)amine; N-[3-chloro-4-[(3-fluorobenzyl)oxy]phenyl]-6-iodo-4-quinazolinamine C21H14ClFIN3O 详情 详情
(XII) 67214 (5-formylfuran-2-yl)boronic acid 27329-70-0 C5H5BO4 详情 详情
(XIII) 49879 5-(4-[3-chloro-4-[(3-fluorobenzyl)oxy]anilino]-6-quinazolinyl)-2-furaldehyde C26H17ClFN3O3 详情 详情
Extended Information