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Sodium Iodide → HCID 11331321, 화합물

HRID 915288
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HRID 915288 반응식
Cl[CH2:2][O:3][C:4](=[O:31])[N:5]([C:28](=[O:30])[CH3:29])[CH2:6][C@@H:7]1[O:11][C:10](=[O:12])[N:9]([C:13]2[CH:18]=[CH:17][C:16]([CH:19]3[CH2:24][CH2:23][S:22](=[O:26])(=[O:25])[CH2:21][CH2:20]3)=[C:15]([F:27])[CH:14]=2)[CH2:8]1.[I-].[Na+].[Cs].[C:35]([N:42]1[CH2:50][CH2:49][CH:45]([C:46]([OH:48])=[O:47])[CH2:44][CH2:43]1)([O:37][C:38]([CH3:41])([CH3:40])[CH3:39])=[O:36]>C(#N)C>[C:38]([O:37][C:35]([N:42]1[CH2:50][CH2:49][CH:45]([C:46]([O:48][CH2:2][O:3][C:4](=[O:31])[N:5]([C:28](=[O:30])[CH3:29])[CH2:6][C@@H:7]2[O:11][C:10](=[O:12])[N:9]([C:13]3[CH:18]=[CH:17][C:16]([CH:19]4[CH2:24][CH2:23][S:22](=[O:26])(=[O:25])[CH2:21][CH2:20]4)=[C:15]([F:27])[CH:14]=3)[CH2:8]2)=[O:47])[CH2:44][CH2:43]1)=[O:36])([CH3:41])([CH3:39])[CH3:40]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 5238Sodium IodideHCID 3928711-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 5354618CesiumHCID 58958555HCID 58958555, 화합물

생성물 1

HCID 11331321HCID 11331321, 화합물수율 72%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

To (R)-acetyl-{3-[4-(1,1-dioxo-hexahydro-1λ6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamic acid chloromethyl ester (10) (751.8 mg, 1.58 mmol) and sodium iodide (236.0 mg, 1.58 mmol) in acetonitrile (30 mL), is added the cesium salt of N-BOC-isonipecotic acid (884.2 mg, 2.45 mmol). The mixture is heated to reflux overnight. After cooling to RT, the mixture is filtered and washed with dichloromethane. The filtrate is diluted with CH2Cl2 and water and the layers are separated. The aq layer is extracted with dichloromethane twice and the combined organic layers are washed with water, brine, dried over sodium sulfate and conc in vacuo. Purification by silica gel chromatography gave the title compound in 72% yield (757.3 mg, 1.13 mmol). 1H NMR (400 MHz, CDCl3): δ 7.47 (dd, 1H), 7.24 (t, 1H), 7.14 (dd, 1H), 5.88 (s, 2H), 4.78-4.85 (m, 1H), 4.18 (dd, 1H), 4.08 (t, 2H), 4.03 (dd, 2H), 3.67 (dd, 1H), 3.13-3.20 (m, 4H), 3.10 (dt, 1H), 2.83 (t, 2H), 2.60 (tt, 1H), 2.59 (s, 3H), 2.35-2.46 (m, 2H), 2.17-2.23 (m, 2H), 1.90-1.96 (m, 2H), 1.57-1.686 (m, 2H) 1.45 (s, 9H). MS-APCI (m/z+): 570.

후처리

  1. temperatureThe mixture is heated
  2. temperatureto reflux overnight
  3. filtrationthe mixture is filtered
  4. washwashed with dichloromethane
  5. additionThe filtrate is diluted with CH2Cl2 and water
  6. customthe layers are separated
  7. extractionThe aq layer is extracted with dichloromethane twice
  8. washthe combined organic layers are washed with water, brine
  9. dry with materialdried over sodium sulfate and conc in vacuo
  10. customPurification by silica gel chromatography

출처 및 근거

ORD 기록
ord-2264161bb69e4f4ba47f5eee1133f0ec
출처 데이터셋
uspto-grants-2007_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07265140B2

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