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【结 构 式】

【分子编号】45678

【品名】tert-butyl (E)-3-[4-(2-[4-[(E)-3-(hexadecylamino)-3-oxo-1-propenyl]phenyl]-2-oxoacetyl)phenyl]-2-propenoate

【CA登记号】

【 分 子 式 】C40H55NO5

【 分 子 量 】629.88044

【元素组成】C 76.27% H 8.8% N 2.22% O 12.7%

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:(V)

Heck reaction of 4,4'-dibromobenzil (VI) with tert-butyl acrylate (III) in the presence of palladium diacetate and tri(o-tolyl)phosphine afforded the arylacrylate ester (VII), which was subsequently condensed with the acrylamide (X) (prepared from acryloyl chloride (VIII) and hexadecylamine (IX)), to furnish adduct (XI). The condensation of diketone (XI) with aldehyde (V) in the presence of ammonium acetate in HOAc produced imidazole (XII). The tert-butyl ester groups of (XII) were finally cleaved by treatment with trifluoroacetic acid.

1 Slee, D.H.; et al.; Development of potent non-carbohydrate imidazole-based small molecule selectin inhibitors antiinflammatory activity. J Med Chem 2001, 44, 13, 2094.
2 Kondo, H.; Inoue, Y.; Jones, T.K.; Ripka, W.C.; Yu, J.; Raheja, R.K.; Nguyen, T.N.; Slee, D.H. (NV Organon; Ontogen Corp.); Substd. thiazoles for treatment of human diseases involving modulators of P-, L- and E-selectin. WO 0033836; WO 0034255 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(III) 12760 tert-butyl acrylate 1663-39-4 C7H12O2 详情 详情
(V) 45678 tert-butyl (E)-3-[4-(2-[4-[(E)-3-(hexadecylamino)-3-oxo-1-propenyl]phenyl]-2-oxoacetyl)phenyl]-2-propenoate C40H55NO5 详情 详情
(VI) 38940 1,2-bis(4-bromophenyl)-1,2-ethanedione 35578-47-3 C14H8Br2O2 详情 详情
(VII) 45675 tert-butyl (E)-3-[4-[2-(4-bromophenyl)-2-oxoacetyl]phenyl]-2-propenoate C21H19BrO4 详情 详情
(VIII) 11577 Acryloyl chloride; Acrylyl chloride;2-Propenoyl chloride 814-68-6 C3H3ClO 详情 详情
(IX) 45676 1-Aminohexadecane; n-Hexadecylamine; Palmitylamine; Cetylamine; hexadecylamine; 1-hexadecanamine 143-27-1 C16H35N 详情 详情
(X) 45677 N-hexadecylacrylamide C19H37NO 详情 详情
(XI) 45674 tert-butyl 3-(4-formylphenyl)-4,5-dihydro-5-isoxazolecarboxylate C15H17NO4 详情 详情
(XII) 45679 tert-butyl 3-[4-(4-[4-[(E)-3-(tert-butoxy)-3-oxo-1-propenyl]phenyl]-5-[4-[(E)-3-(hexadecylamino)-3-oxo-1-propenyl]phenyl]-1H-imidazol-2-yl)phenyl]-4,5-dihydro-5-isoxazolecarboxylate C55H72N4O6 详情 详情
Extended Information