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【结 构 式】

【分子编号】31426

【品名】4-[4-(tert-butoxycarbonyl)-1-piperazinyl]benzoic acid

【CA登记号】

【 分 子 式 】C16H22N2O4

【 分 子 量 】306.36176

【元素组成】C 62.73% H 7.24% N 9.14% O 20.89%

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:(X)

The condensation of L-asparagine (I) with benzenesulfonyl chloride (II) in the presence of NaOH gave sulfonamide (III). Subsequent Hofmann rearrangement of (III) employing sodium hypobromite produced the diaminopropionic acid derivative (IV), which was protected as the tert-butyl ester (V) using isobutylene in the presence of H2SO4. Condensation of methyl 4-aminobenzoate (VI) with bis(2-chloroethyl)amine (VII) in refluxing butanol yielded the arylpiperazine (VIII), which was protected with di tert-butyl dicarbonate to give the corresponding carbamate (IX). Basic hydrolysis of the methyl ester of (IX) provided carboxylic acid (X). This was then coupled with amine (V) using benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (BOP) to afford amide (XI). Finally, deprotection of the tert-butyl ester and BOC group of (XI) with trifluoroacetic acid furnished the title compound.

1 Egbertson, M.S.; Turchi, L.M.; Hartman, G.D.; Halczenko, W.; Whitman, D.B.; Perkins, J.J.; Krause, A.E.; Ihle, N.; Claremon, D.A.; Hoffman, W.; Duggan, M.E. (Merck & Co., Inc.); Fibrinogen receptor antagonists. EP 0673247; JP 1996504194; WO 9412181 .
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) 25972 S-(+)-Asparagine; S-(+)-2-Aminosuccinamic acid; L-Asparagine 70-47-3 C4H8N2O3 详情 详情
(II) 14713 benzenesulfonyl chloride 98-09-9 C6H5ClO2S 详情 详情
(III) 25973 (2S)-4-amino-4-oxo-2-[(phenylsulfonyl)amino]butyric acid C10H12N2O5S 详情 详情
(IV) 31422 (2S)-3-amino-2-[(phenylsulfonyl)amino]propionic acid C9H12N2O4S 详情 详情
(V) 31423 tert-butyl (2S)-3-amino-2-[(phenylsulfonyl)amino]propanoate C13H20N2O4S 详情 详情
(VI) 20537 methyl 4-aminobenzoate 619-45-4 C8H9NO2 详情 详情
(VII) 21583 2-chloro-N-(2-chloroethyl)-1-ethanamine; Bis(2-chloroethyl)amine; 1,1'-iminobis(2-chloroethane); N,N-bis(2-chloroethyl)amine 821-48-7 C4H9Cl2N 详情 详情
(VIII) 31424 methyl 4-(1-piperazinyl)benzoate C12H16N2O2 详情 详情
(IX) 31425 tert-butyl 4-[4-(methoxycarbonyl)phenyl]-1-piperazinecarboxylate C17H24N2O4 详情 详情
(X) 31426 4-[4-(tert-butoxycarbonyl)-1-piperazinyl]benzoic acid C16H22N2O4 详情 详情
(XI) 31427 tert-butyl 4-[4-[([(2S)-3-(tert-butoxy)-3-oxo-2-[(phenylsulfonyl)amino]propyl]oxy)carbonyl]phenyl]-1-piperazinecarboxylate C29H39N3O8S 详情 详情
Extended Information