【结 构 式】 |
【分子编号】43384 【品名】3-[(3S)-1-propylpiperidinyl]phenylamine; 3-[(3S)-1-propylpiperidinyl]aniline 【CA登记号】 |
【 分 子 式 】C14H22N2 【 分 子 量 】218.34216 【元素组成】C 77.01% H 10.16% N 12.83% |
合成路线1
该中间体在本合成路线中的序号:(IV)The reaction of 3-(1-propylpiperidin-3(S)-yl)phenol (I) with trifluoromethanesulfonic anhydride gives the triflate (II), which is treated with Pd(OAc)4, CO and MeOH, yielding 3-(1-propylpiperidin-3(S)-yl)benzoic acid methyl ester (III). The reaction of (III) with sodium azide and H2SO4 affords the aniline (IV), which by reaction with NaNO2, HBr and CuBr provides 3(S)-(3-bromophenyl)-1-propylpiperidine (V). The reaction of (V) with dimethyl disulfide and n-BuLi gives the thioether (VI), which is oxidized with MCPBA to afford the target sulfone, which is easily separated from the N-oxide (VII) also formed in the oxidation process. The N-oxide (VII) can be reduced to the target compound by means of TiCl4 and NaI in acetonitrile.
【1】 Sonesson, C.; et al.; Substituted (S)-phenylpiperidines and rigid congeners as preferential dopamine autoreceptor antagonists: Synthesis and structure-activity relationships. J Med Chem 1994, 37, 17, 2735. |
【2】 Svensson, K.A.I.; Wikström, H.V.; Carlsson, P.A.E.; Boije, A.M.P.; Waters, R.N.; Sonesson, C.A.; Stjerulof, N.P.; Andersson, B.R. (Pharmacia Corp.); New centrally acting substd. phenylazacycloalkanes. EP 0641320; JP 1994509561; US 5462947; WO 9218475 . |
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) | 43381 | 3-[(3S)-1-propylpiperidinyl]phenol | C14H21NO | 详情 | 详情 | |
(II) | 43382 | 3-[(3S)-1-propylpiperidinyl]phenyl trifluoromethanesulfonate | C15H20F3NO3S | 详情 | 详情 | |
(III) | 43383 | methyl 3-[(3S)-1-propylpiperidinyl]benzoate | C16H23NO2 | 详情 | 详情 | |
(IV) | 43384 | 3-[(3S)-1-propylpiperidinyl]phenylamine; 3-[(3S)-1-propylpiperidinyl]aniline | C14H22N2 | 详情 | 详情 | |
(V) | 43385 | (3S)-3-(3-bromophenyl)-1-propylpiperidine | C14H20BrN | 详情 | 详情 | |
(VI) | 43386 | (3S)-3-[3-(methylsulfanyl)phenyl]-1-propylpiperidine; methyl 3-[(3S)-1-propylpiperidinyl]phenyl sulfide | C15H23NS | 详情 | 详情 | |
(VII) | 43387 | (3S)-3-[3-(methylsulfonyl)phenyl]-1-propyl-1-piperidiniumolate | C15H23NO3S | 详情 | 详情 |