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【结 构 式】 
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【分子编号】46323 【品名】(R)-1,3-benzothiazol-2-yl[(2S)pyrrolidinyl]methanol 【CA登记号】 |
【 分 子 式 】C12H14N2OS 【 分 子 量 】234.32204 【元素组成】C 61.51% H 6.02% N 11.96% O 6.83% S 13.68% |
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)Condensation of the Weinreb amide of N-Boc-proline (I) with the lithium anion of benzothiazole (II) in THF at -78 C gave benzothiazolyl ketone (III), which was reduced with NaBH4 to afford the diastereomeric mixture of alcohols (IV). Deprotection of the Boc group of (IV) by means of HCl in EtOAc provided pyrrolidine (V). This was then coupled with Z-leucyl-glycine (VI) in the presence of PyBOP to give the peptidyl alcohol (VII). Finally, Swern oxidation of (VII) furnished the corresponding ketone.
| 【1】 Santana, J.; Gullet, C.; Schrével, J.; Frappier, F.; Maoulida, C.; Grellier, P.; Joyeau, R.; Teixeira, A.R.L.; Synthesis and activity of pyrrolidinyl- and thiazolidinyl-dipeptide derivatives as inhibitors of the Tc80 prolyl oligopeptidase from Trypanosoma cruzi. Eur J Med Chem 2000, 35, 2, 257. |
| 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) | 46320 | tert-butyl (2S)-2-[[methoxy(methyl)amino]carbonyl]-1-pyrrolidinecarboxylate | C12H22N2O4 | 详情 | 详情 | |
| (II) | 36784 | 1,3-benzothiazole | 95-16-9 | C7H5NS | 详情 | 详情 |
| (III) | 46321 | tert-butyl (2S)-2-(1,3-benzothiazol-2-ylcarbonyl)-1-pyrrolidinecarboxylate | C17H20N2O3S | 详情 | 详情 | |
| (IV) | 46322 | tert-butyl (2S)-2-[(R)-1,3-benzothiazol-2-yl(hydroxy)methyl]-1-pyrrolidinecarboxylate | C17H22N2O3S | 详情 | 详情 | |
| (V) | 46323 | (R)-1,3-benzothiazol-2-yl[(2S)pyrrolidinyl]methanol | C12H14N2OS | 详情 | 详情 | |
| (VI) | 46318 | 2-[((2S)-2-[[(benzyloxy)carbonyl]amino]-4-methylpentanoyl)amino]acetic acid | C16H22N2O5 | 详情 | 详情 | |
| (VII) | 46324 | benzyl (1S)-1-[[(2-[(2S)-2-[(R)-1,3-benzothiazol-2-yl(hydroxy)methyl]pyrrolidinyl]-2-oxoethyl)amino]carbonyl]-3-methylbutylcarbamate | C28H34N4O5S | 详情 | 详情 |
Extended Information