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【结 构 式】

【分子编号】23641

【品名】2-methoxy-1-phenyl-1-ethanone

【CA登记号】4079-52-1

【 分 子 式 】C9H10O2

【 分 子 量 】150.1772

【元素组成】C 71.98% H 6.71% O 21.31%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(II)

Condensation of isatin (I) with 2-methoxyacetophenone (II) in the presence of KOH afforded quinolinecarboxylic acid (III). Subsequent demethylation of the ether function of (III) with refluxing 57% HI gave (IV), which was then condensed with (S)-1-phenylpropyl amine (V) using DCC and HOBt to yield the title amide.

1 Giardina, G.A.M.; et al.; Discovery of a novel class of selective non-peptid. J Med Chem 1999, 42, 6, 1053.
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) 14098 2,3-Indolinedione; 1H-Indole-2,3-dione; Isatin 91-56-5 C8H5NO2 详情 详情
(II) 23641 2-methoxy-1-phenyl-1-ethanone 4079-52-1 C9H10O2 详情 详情
(III) 23642 3-methoxy-2-phenyl-4-quinolinecarboxylic acid C17H13NO3 详情 详情
(IV) 23643 3-hydroxy-2-phenyl-4-quinolinecarboxylic acid 485-89-2 C16H11NO3 详情 详情
(V) 23644 (1S)-1-phenylpropylamine; (1S)-1-phenyl-1-propanamine 3789-59-1 C9H13N 详情 详情

合成路线2

该中间体在本合成路线中的序号:(II)

The quinolinecarboxylic acid (III) was obtained by the Pfitzinger reaction of isatin (I) with 2-methoxyacetophenone (II) in ethanolic KOH at 80 C. Subsequent methyl ether cleavage in (III) using concentrated HI provided 3-hydroxy-2-phenylquinoline-4-carboxylic acid (IV). Coupling of acid (IV) with (S)-1-phenylpropylamine (V) by means of DCC and HOBt gave amide (VI). Ester (VIII) was then obtained by alkylation of the 3-hydroxy quinoline (VI) with ethyl bromoacetate (VII) in the presence of K2CO3 and KI. Finally, hydrolysis of the ethyl ester (VIII) with refluxing HCl afforded the corresponding carboxylic acid.

1 Giardina, G.A.M.; et al.; Discovery of a novel class of selective non-peptid. J Med Chem 1999, 42, 6, 1053.
2 Giardina, G.A.M.; Grugni, M.; Raveglia, L.F.; Farino, C. (GlaxoSmithKline plc); Quinoline derivs.. EP 0876347; JP 2000501104; US 6277862; WO 9721680 .
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) 14098 2,3-Indolinedione; 1H-Indole-2,3-dione; Isatin 91-56-5 C8H5NO2 详情 详情
(II) 23641 2-methoxy-1-phenyl-1-ethanone 4079-52-1 C9H10O2 详情 详情
(III) 23642 3-methoxy-2-phenyl-4-quinolinecarboxylic acid C17H13NO3 详情 详情
(IV) 23643 3-hydroxy-2-phenyl-4-quinolinecarboxylic acid 485-89-2 C16H11NO3 详情 详情
(V) 23644 (1S)-1-phenylpropylamine; (1S)-1-phenyl-1-propanamine 3789-59-1 C9H13N 详情 详情
(VI) 58526 3-hydroxy-2-phenyl-N-[(1S)-1-phenylpropyl]-4-quinolinecarboxamide C25H22N2O2 详情 详情
(VII) 16640 Ethyl 2-bromoacetate; Ethyl bromoacetate 105-36-2 C4H7BrO2 详情 详情
(VIII) 58527 ethyl 2-{[2-phenyl-4-({[(1S)-1-phenylpropyl]amino}carbonyl)-3-quinolinyl]oxy}acetate C29H28N2O4 详情 详情
Extended Information