• English
  • 简体中文
Login Register
Current Location: Home > Feedback Help Print

【结 构 式】

【分子编号】14297

【品名】tert-butyl 4-[2-(2-amino-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-6-yl)ethynyl]benzoate

【CA登记号】

【 分 子 式 】C20H18N4O3

【 分 子 量 】362.38808

【元素组成】C 66.29% H 5.01% N 15.46% O 13.24%

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:(XXI)

Alternative preparation of the key intermediote (XIII)

1 Harrington, P.M.; Shih, C.; Grindey, G.B.; Gossett, L.S.; Moran, R.G.; Taylor, S.C.; Synthesis and structure-activity relationship studies of 5,10-dideazatetrahydrofolic acid (DDATHF). Chemistry and Biology of Pteridines (1989): Pteridines and Folic Acid Derivatives. H.-C. Curtius, S. Ghisla and N. Blau (Eds.). de Gruyter, New York 1990, 1035.
2 Taylor, E.C.; Wong, G.S.K.; Convergent and efficient palladium-effected synthesis of 5,10-dideaza-5,6,7,8-tetrahydrofolic acid (DDATHF). J Org Chem 1989, 54, 15, 3618.
3 Castaner, J.; Prous, J.; Lometrexol. Drugs Fut 1993, 18, 2, 121.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
14790 Guanidine 113-00-8 CH5N3 详情 详情
63827 1-iodo-2,5-pyrrolidinedione C4H4INO2 详情 详情
(XVI) 14292 methyl 2-oxo-1,2-dihydro-3-pyridinecarboxylate C7H7NO3 详情 详情
(XVII) 14293 methyl 5-iodo-2-oxo-1,2-dihydro-3-pyridinecarboxylate C7H6INO3 详情 详情
(XVIII) 14294 methyl 2-chloro-5-iodonicotinate C7H5ClINO2 详情 详情
(XIX) 14285 tert-butyl 4-ethynylbenzoate C13H14O2 详情 详情
(XX) 14296 methyl 5-[2-[4-(tert-butoxycarbonyl)phenyl]ethynyl]-2-chloronicotinate C20H18ClNO4 详情 详情
(XXI) 14297 tert-butyl 4-[2-(2-amino-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-6-yl)ethynyl]benzoate C20H18N4O3 详情 详情
(XXII) 14298 4-[2-(2-Amino-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-6-yl)ethynyl]benzoic acid C16H10N4O3 详情 详情
Extended Information