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【结 构 式】

【分子编号】66043

【品名】 

【CA登记号】 

【 分 子 式 】C13H17N3OS

【 分 子 量 】263.3636

【元素组成】C 59.29% H 6.51% N 15.96% O 6.08% S 12.18%

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:(VII)

Cenicriviroc mesilate can be prepared by two related strategies:
In one strategy, chlorination of benzazocine-5-carboxylic acid derivative (I) with (COCl)2 (1, 2) or SOCl2 in THF (3) yields the corresponding acyl chloride (II) (1-3), which then couples with S-Cbz-4-thioaniline (III) in the presence of Et3N in THF to afford, after hydrolysis of the Cbz group with NaOH in MeOH, the corresponding N-(4-sulfanylphenyl)amide (IV). Subsequent S-alkylation of thiol (IV) with 5-(chloromethyl)-1-propylimidazole (V) in the presence of NaOH in MeOH yields thioether (VI). After oxidation of (VI) with mCPBA in CH2Cl2, the resulting racemic sulfoxide is resolved employing chiral HPLC to furnish the target (S)-enantiomer, which is then treated with MsOH in EtOAc to afford cenicriviroc mesilate (2). In another strategy, acyl chloride (II) couples with the substituted aniline (VII) in the presence of DIEA in THF (1) or Et3N in THF (3) to yield cenicriviroc, which is then reacted with MsOH in methyl isobutyl ketone, producing the target cenicriviroc mesilate (1, 3). Scheme 1.

1 Nishiguchi, A., Adachi, M., Ito, T., Ikemoto, T., Tawada, H. (Takeda Pharmaeutical Co., Ltd.). Process for producing optically active sulfoxide derivative. CA 2479071, EP 1484322, JP 2004123694, WO 2003076411.
2 Shiraishi, M., Baba, M., Iizawa, Y., Kanzaki, N., Seto, M., Aikawa, K. (Takeda Pharmaceutical Co., Ltd.). Bicyclic compounds, production and use thereof. CA 2459172, CA 2607992, EP 1423376, EP 1889839, EP 2206702, JP 2003335776, JP 2007084578, JP 2009209154, US 2004259876, US 7371772, US 2008161287, US 2009030032, WO 2003014105.
3 Seto, M., Aikawa, K., Miyamoto, N. et al. Highly potent and orally active CCR5 antagonists as Anti-HIV-1 agents: Synthesis and biological activities of 1-benzazocine derivatives containing a sulfoxide moiety. J Med Chem 2006, 49(6): 2037-48.
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) 66037     C28H37NO4 详情 详情
(II) 66038     C28H36ClNO3 详情 详情
(III) 66039     C14H13NO2S 详情 详情
(IV) 66040     C34H42N2O3S 详情 详情
(V) 66041 5-(chloromethyl)-1-propylimidazole   C7H11ClN2 详情 详情
(VI) 66042     C41H52N4O3S 详情 详情
(VII) 66043     C13H17N3OS 详情 详情

合成路线2

该中间体在本合成路线中的序号:(VII)

Synthesis of intermediate (VII):
Reaction of 4-sulfanylaniline (XX) with TFAA in the presence of Et3N in THF gives trifluoroacetamide (XXI), which then condenses with 5-(chloromethyl)-1-propylimidazole (V) using TEA in MeOH/H2O to yield thioether (XXII). Oxidation of sulfanyl derivative (XXII) by means of H2O2 in AcOH, followed by hydrolysis with NaOH affords the racemic sulfinyl derivative (XXIII), which is then submitted to optical resolution with di-p-toluoyl-D-tartaric acid to provide the desired (S)-enantiomer (VII) (1). Scheme 3.

1 Nishiguchi, A., Adachi, M., Ito, T., Ikemoto, T., Tawada, H. (Takeda Pharmaeutical Co., Ltd.). Process for producing optically active sulfoxide derivative. CA 2479071, EP 1484322, JP 2004123694, WO 2003076411.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(V) 66041 5-(chloromethyl)-1-propylimidazole   C7H11ClN2 详情 详情
(VII) 66043     C13H17N3OS 详情 详情
(XX) 16490 4-aminophenylhydrosulfide; 4-aminothiophenol; 4-aminobenzenethiol 1193-02-8 C6H7NS 详情 详情
(XXI) 66054 2,2,2-Trifluoro-N-(4-Mercaptophenyl)Acetamide; 2,2,2-Trifluoro-N-(4-Sulfanylphenyl)Ethanamide 94006-35-6 C8H6F3NOS 详情 详情
(XXII) 66055     C15H16F3N3OS 详情 详情
(XXIII) 66056     C13H17N3OS 详情 详情
Extended Information