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【结 构 式】

【分子编号】34628

【品名】methyl 2-[[(2S)-2-[[(benzyloxy)carbonyl]amino]-3-(1-trityl-1H-imidazol-4-yl)propanoyl][(1R)-1-phenylethyl]amino]acetate

【CA登记号】

【 分 子 式 】C44H42N4O5

【 分 子 量 】706.84144

【元素组成】C 74.77% H 5.99% N 7.93% O 11.32%

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)

The alkylation of (R)-alpha-methylbenzylamine (I) with methyl bromoacetate (II) gave aminoacetate (III). This was coupled with protected histidine (IV) by means of HATU as the coupling agent, yielding the protected dipeptide (V). Subsequent saponification of (V) using LiOH gave acid (VI). beta,beta-Dimethyl-phenethylamine (IX) was prepared by alkylation of phenylacetonitrile (VII) with iodomethane and NaH, followed by hydrogenation of the resulting dimethylated compound (VIII) in the presence of Raney Nickel. Coupling of amine (IX) with dipeptide (VI) provided the corresponding amide (X). The trityl protecting group of (X) was finally removed by treatment with trifluoroacetic acid.

1 Doherty, A.M.; Quin, J. III; Kaltenbronn, J.S.; Leonard, D.M.; McNamara, D.J. (Pfizer Inc.); Functionalized alkyl and alkenyl side chain derivs. of glycinamides as farnesyl transferase inhibitors. WO 9955725 .
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) 10039 (1R)-1-Phenylethylamine; (1R)-1-Phenyl-1-ethanamine.; L-alpha-Phenylethylamine 3886-69-9 C8H11N 详情 详情
(II) 12309 methyl 2-bromoacetate; methyl bromoacetate 96-32-2 C3H5BrO2 详情 详情
(III) 34626 methyl 2-[[(1R)-1-phenylethyl]amino]acetate C11H15NO2 详情 详情
(IV) 34627 (2S)-2-[[(benzyloxy)carbonyl]amino]-3-(1-trityl-1H-imidazol-4-yl)propionic acid C33H29N3O4 详情 详情
(V) 34628 methyl 2-[[(2S)-2-[[(benzyloxy)carbonyl]amino]-3-(1-trityl-1H-imidazol-4-yl)propanoyl][(1R)-1-phenylethyl]amino]acetate C44H42N4O5 详情 详情
(VI) 34629 2-[[(2S)-2-[[(benzyloxy)carbonyl]amino]-3-(1-trityl-1H-imidazol-4-yl)propanoyl][(1R)-1-phenylethyl]amino]acetic acid C43H40N4O5 详情 详情
(VII) 17046 Phenylacetonitrile; 2-phenylacetonitrile; Benzyl cyanide 140-29-4 C8H7N 详情 详情
(VIII) 34630 2-methyl-2-phenylpropanenitrile C10H11N 详情 详情
(IX) 34631 2-methyl-2-phenylpropylamine; 2-methyl-2-phenyl-1-propanamine C10H15N 详情 详情
(X) 34632 benzyl (1S)-2-[[2-[(2-methyl-2-phenylpropyl)amino]-2-oxoethyl][(1R)-1-phenylethyl]amino]-2-oxo-1-[(1-trityl-1H-imidazol-4-yl)methyl]ethylcarbamate C53H53N5O4 详情 详情
Extended Information