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【结 构 式】

【分子编号】45858

【品名】diethyl 2-[2-(4-pyridinyl)ethyl]malonate

【CA登记号】

【 分 子 式 】C14H19NO4

【 分 子 量 】265.3092

【元素组成】C 63.38% H 7.22% N 5.28% O 24.12%

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:(XVIII)

Intermediate (VII) can be obtained by following two different pathways: 1. Hydrogenation of 4-pyridine acetic acid (IX) over PtO2 in AcOH affords piperidinyl derivative (X), which is then protected with Boc2O and NaOH in THF to yield (XI). Reduction of the CO2H group of (XI) with BH3.THF in THF gives alcohol (XII), which is then subjected to Swern oxidation with oxalyl chloride and DMSO in CH2Cl2, followed by reaction with Wittig reagent (XIII) and N-methyl morpholine (NMM), to provide crotonate (XIV). Hydrogenation of (XIV) over Pd/C in MeOH furnishes methyl butyrate (XV), which is finally hydrolyzed with NaOH in MeOH. 2. Alternatively, intermediate (VII) can be obtained by reaction of diethyl malonate (XVI) with 4-vinylpyridine and NaH in EtOH to afford derivative (XVIII), which is hydrolyzed and decarboxylated with HCl/H2O and then hydrogenated over PtO2 to provide piperidine derivative (XIX). Finally, (XIX) is protected by reaction with Boc2O and NaOH in THF.

1 Molino, B.F.; Klein, S.I.; Czekaj, M.; et al.; Design of a new class of orally active fibrinogen receptor antagonists. J Med Chem 1998, 41, 14, 2492.
2 Klein, S.I.; Molino, B.F. (Aventis Pharma SA); Antithrombotic azacycloalkylalkanoyl peptides and pseudopeptides. EP 0812205; JP 1997507213; US 5866685; WO 9510295 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(VII) 45852 4-[1-(tert-butoxycarbonyl)-4-piperidinyl]butyric acid C14H25NO4 详情 详情
(IX) 17883 2-(4-pyridinyl)acetic acid 28356-58-3 C7H7NO2 详情 详情
(X) 45854 2-(4-piperidinyl)acetic acid; 4-piperidinylacetic acid 51052-78-9 C7H13NO2 详情 详情
(XI) 19346 1-Boc-piperidin-4-ylacetic acid; 2-[1-(tert-butoxycarbonyl)-4-piperidinyl]acetic acid 157688-46-5 C12H21NO4 详情 详情
(XII) 43453 tert-butyl 4-(2-hydroxyethyl)-1-piperidinecarboxylate C12H23NO3 详情 详情
(XIII) 14689 Methyl (triphenylphosphoranylidene)acetate; (methoxycarbonylmethylene)triphenylphosphorane;Methyl 2-(triphenyl-lambda(5)-phosphanylidene)acetate 2605-67-6 C21H19O2P 详情 详情
(XIV) 45855 tert-butyl 4-[(E)-4-methoxy-4-oxo-2-butenyl]-1-piperidinecarboxylate C15H25NO4 详情 详情
(XV) 45856 tert-butyl 4-(4-methoxy-4-oxobutyl)-1-piperidinecarboxylate C15H27NO4 详情 详情
(XVI) 16829 Diethyl malonate 105-53-3 C7H12O4 详情 详情
(XVII) 45857 4-vinylpyridine C7H7N 详情 详情
(XVIII) 45858 diethyl 2-[2-(4-pyridinyl)ethyl]malonate C14H19NO4 详情 详情
(XIX) 45859 4-(4-piperidinyl)butyric acid C9H17NO2 详情 详情
Extended Information