2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbaldehyde -Drug Synthesis Database

【结构式】

【分子编号】14270

【品名】2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbaldehyde

【CA登记号】

【分子式】C₈H₇N₅O

【分子量】189.17668

【元素组成】C 50.79% H 3.73% N 37.02% O 8.46%

与该中间体有关的原料药合成路线共 2 条

合成路线1 合成路线2

合成路线1

该中间体在本合成路线中的序号：(II)

Racemic lometrexol has been prepared.

参考文献中间体

合成目标

【1】 Okazaki, S.; Asao, T.; Wakida, M.; Ishida, K.; Washinosu, M.; Utsugi, T.; Yamada, Y. (Taiho Pharmaceutical Co., Ltd.); Novel fused indan deriv. and pharmaceutically acceptable salt. EP 0713870; US 5710162; US 5733918; WO 9532187 .
【2】 Castaner, J.; Prous, J.; Lometrexol. Drugs Fut 1993, 18, 2, 121.

中间体序号	中间体编号	品名	分子式	供应商	用于合成
(VI*)	11013	diethyl (2S)-2-aminopentanedioate	C₉H₁₇NO₄	详情	详情
(I)	14269	2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbonitrile	C₈H₆N₆	详情	详情
(II)	14270	2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbaldehyde	C₈H₇N₅O	详情	详情
(III)	14271	[4-(Methoxycarbonyl)benzyl](diphenyl)phosphonium	C₂₁H₂₀O₂P	详情	详情
(IV)	14272	methyl 4-[(E)-2-(2,4-diaminopyrido[2,3-d]pyrimidin-6-yl)ethenyl]benzoate	C₁₇H₁₅N₅O₂	详情	详情
(V)	14273	4-[(E)-2-(2-Amino-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-6-yl)ethenyl]benzoic acid	C₁₆H₁₂N₄O₃	详情	详情
(VII)	14275	diethyl (2S)-2-([4-[(E)-2-(2-amino-4-oxo-3,4-dihydropyrido[2,3-d]pyrimidin-6-yl)ethenyl]benzoyl]amino)pentanedioate	C₂₅H₂₇N₅O₆	详情	详情
(VIII)	14276	diethyl (2S)-2-([4-[2-(2-amino-4-oxo-3,4,5,6,7,8-hexahydropyrido[2,3-d]pyrimidin-6-yl)ethyl]benzoyl]amino)pentanedioate	C₂₅H₃₃N₅O₆	详情	详情

合成路线2

该中间体在本合成路线中的序号：(VII)

Pyridine (III) was prepared by condensation of malononitrile (I) with triethyl orthoformate (II) in refluxing pyridine, followed by treatment with concentrated HCl. Dechlorination of (III) was effected by hydrogenolysis in the presence of Pd on BaCO3. The dechlorinated pyridine dinitrile (IV) was cyclized with guanidine (V), yielding the pyridopyrimidine (VI). Reduction of the nitrile function of (VI) to aldehyde (VII) was carried out using formic acid and Raney-Ni. This was further reduced to alcohol (VIII) with NaBH4. Bromination of the alcohol (VIII) by means of HBr resulted in bromide (IX). Nucleophilic displacement of the bromide group of (IX) with the sodium salt of 1-naphthalenethiol (X) afforded the target sulfide.

参考文献中间体

合成目标

【1】 Gangjee, A.; et al.; Synthesis of 2,4-diamino-6-(thioarylmethyl)pyrido [2,3-d]pyrimidines as dihydrofolate reductase inhibitors. Bioorg Med Chem 2001, 9, 11, 2929.

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)	12061	Malononitrile	109-77-3	C₃H₂N₂	详情	详情
(II)	21304	Triethyl orthoformate; 1-(Diethoxymethoxy)ethane; Diethoxymethyl ethyl ether	122-51-0	C₇H₁₆O₃	详情	详情
(III)	50364	2-amino-6-chloro-3,5-pyridinedicarbonitrile		C₇H₃ClN₄	详情	详情
(IV)	31544	2-amino-3,5-pyridinedicarbonitrile		C₇H₄N₄	详情	详情
(V)	14790	Guanidine	113-00-8	CH₅N₃	详情	详情
(VI)	14269	2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbonitrile		C₈H₆N₆	详情	详情
(VII)	14270	2,4-Diaminopyrido[2,3-d]pyrimidine-6-carbaldehyde		C₈H₇N₅O	详情	详情
(VIII)	50365	(2,4-diaminopyrido[2,3-d]pyrimidin-6-yl)methanol		C₈H₉N₅O	详情	详情
(IX)	50366	2-amino-6-(bromomethyl)pyrido[2,3-d]pyrimidin-4-ylamine; 6-(bromomethyl)pyrido[2,3-d]pyrimidine-2,4-diamine		C₈H₈BrN₅	详情	详情
(X)	50367	1-Naphthalenethiol	529-36-2	C₁₀H₈S	详情	详情

Extended Information