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【结 构 式】

【分子编号】66749

【品名】tert-butyl 4-((2-(diethylamino)ethyl)carbamoyl)-3,5-dimethyl-1H-pyrrole-2-carboxylate

【CA登记号】 

【 分 子 式 】C18H31N3O3

【 分 子 量 】337.463

【元素组成】C 64.07% H 9.26% N 12.45% O 14.22%

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:(V)

 

1 Jin QW, Mnuragis MA, May PD. 2003. Process for preparing aminocarbonylpyrrolylmethylideneindolinones from indolinones, imidazolcarbonylpyrrolecarboxaldehydes, and amines. W0 2003070725
2 Manley JM, Kalman MJ, Conway BG, et al. 2003. Early amidation approach to 3-[(4-anudo)pyrrol-2-yl]-2-indolinones. J Org Cbem, 68(16):6447~6450
3 Wang JQ, Miller KD, Sledge GW, et aL. 2005. Synthesis of [18F] SU11248, a new potential PET tracer for imaging cancer tyrosine kinase. Bioorg Med Chem lett, 15(19): 4380~4384
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) 60384 5-fluoro-1,3-dihydro-2H-indol-2-one 56341-41-4 C8H6FNO 详情 详情
(I) 11367 4-Methylene-2-oxetanone; Acetyl ketene 674-82-8 C4H4O2 详情 详情
(II) 66748 N-(2-(diethylamino)ethyl)-3-oxobutanamide   C10H20N2O2 详情 详情
(III) 27907 Acetoacetic acid tert-butyl ester;3-Oxo-butanoic acid 1,1-dimethylethyl estertert-butyl 3-oxobutanoate 1694-31-1 C8H14O3 详情 详情
(IV) 63353 1,1-dimethylethyl 2-(hydroxyimino)-3-oxobutanoate 14352-65-9 C8H13NO4 详情 详情
(V) 66749 tert-butyl 4-((2-(diethylamino)ethyl)carbamoyl)-3,5-dimethyl-1H-pyrrole-2-carboxylate   C18H31N3O3 详情 详情
(VI) 66750 N-(2-(diethylamino)ethyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide   C13H23N3O 详情 详情
(VII) 17643 (Chloromethylene)dimethylammonium chloride; N-(chloromethylene)-N-methylmethanaminium chloride 3724-43-4 C3H7Cl2N 详情 详情
(VIII) 66751 N-((4-((2-(diethylamino)ethyl)carbamoyl)-3,5-dimethyl-1H-pyrrol-2-yl)methylene)-N-methylmethanaminium chloride   C16H29ClN4O 详情 详情
(X) 66752 (Z)-N-[2-(Diethylamino)ethyl]-5-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxamide 326914-13-0 C22H27FN4O2 详情 详情
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