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N-BETA-氨乙基-GAMMA-氨丙基甲基二甲氧基硅烷 → 2-Chloro-4-((1R,2S)-2-hydroxy-1-(5-(3-methoxyphenyl)-1,3,4-oxadiazol-2-yl)propylamino)-3-methylbenzonitrile

HRID 1254635
笔记
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反应方程式

HRID 1254635 反应方程式
[Cl:1][C:2]1[C:3]([CH3:29])=[C:4]([NH:10][C@H:11]([C@@H:26]([OH:28])[CH3:27])[C:12]([NH:14][NH:15][C:16](=O)[C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([O:23][CH3:24])[CH:18]=2)=[O:13])[CH:5]=[CH:6][C:7]=1[C:8]#[N:9].CCN(P1(N(C)CCCN1C)=NC(C)(C)C)CC>C1COCC1>[Cl:1][C:2]1[C:3]([CH3:29])=[C:4]([NH:10][C@@H:11]([C:12]2[O:13][C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([O:23][CH3:24])[CH:18]=3)=[N:15][N:14]=2)[C@@H:26]([OH:28])[CH3:27])[CH:5]=[CH:6][C:7]=1[C:8]#[N:9]
参与物实验过程后处理来源与证据反应笔记

参与物

4

反应物 2

HCID 3513851N-BETA-氨乙基-GAMMA-氨丙基甲基二甲氧基硅烷HCID 67006671N'-((2R,3S)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoyl)-3-methoxybenzohydrazide2 次

产物 1

HCID 442003062-Chloro-4-((1R,2S)-2-hydroxy-1-(5-(3-methoxyphenyl)-1,3,4-oxadiazol-2-yl)propylamino)-3-methylbenzonitrile收率 55%

试剂、催化剂与溶剂 1

HCID 8028四氢呋喃溶剂

实验过程

To a 100 mL round bottom flask was added N′-((2R,3S)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoyl)-3-methoxybenzohydrazide (Intermediate 6a) (441 mg, 1.1 mmol) was added THF (90 mL) and stirred at room temperature. PS-BEMP (1.45 g, 3.2 mmol base) was added to the solution followed by slow addition of p-TSCl (208 mg, 1.1 mmol). The reaction mixture was stirred for 2 h and the progress of the reaction was monitored by TLC. After the completion of the reaction, the BEMP reagent was filtered off, washed with methanol (100 mL), and the resulting solution was concentrated to obtain the crude material. The crude material was chromatographed on silica gel with hexanes:EtOAc (2:8) to get the purified product (232 mg, 55%). 1H NMR (400 MHz, d6-acetone, δ in ppm) 7.42 (m, 1H), 7.33 (m, 3H), 7.01 (m, 1H), 6.50 (d, J=8.7 Hz, 1H), 5.37 (d, J=8.5 Hz, 1H), 4.72 (m, 1H), 4.62 (m, 1H), 3.94 (br s, 1H), 3.80 (s, 3H), 2.37 (s, 3H), 1.43 (d, J=6.4 Hz, 3H).

后处理

  1. additionfollowed by slow addition of p-TSCl (208 mg, 1.1 mmol)
  2. stirringThe reaction mixture was stirred for 2 h
  3. customAfter the completion of the reaction
  4. filtrationthe BEMP reagent was filtered off
  5. washwashed with methanol (100 mL)
  6. concentrationthe resulting solution was concentrated
  7. customto obtain the crude material
  8. customThe crude material was chromatographed on silica gel with hexanes:EtOAc (2:8)

来源与证据

ORD记录
ord-3c88ac01e9764c5ab33ed90d8cf2b1a5
来源数据集
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08455525B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记