Dichloromethane → Tert-butyl cis-2-(6-chloro-5-cyano-3-fluoropyridin-2-ylamino)cyclohexylcarbamate

HRID 2406692노트

반응식

HRID 2406692 반응식
ClC(Cl)(Cl)C(Cl)=O.ClCCl.[NH2:11][C:12]([C:14]1[CH:15]=[C:16]([F:36])[C:17]([NH:21][C@H:22]2[CH2:27][CH2:26][CH2:25][CH2:24][C@H:23]2[NH:28][C:29](=[O:35])[O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[N:18][C:19]=1[Cl:20])=O>C(N(CC)CC)C>[Cl:20][C:19]1[N:18]=[C:17]([NH:21][C@H:22]2[CH2:27][CH2:26][CH2:25][CH2:24][C@H:23]2[NH:28][C:29](=[O:35])[O:30][C:31]([CH3:34])([CH3:32])[CH3:33])[C:16]([F:36])=[CH:15][C:14]=1[C:12]#[N:11]

참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 6420Trichloroacetyl chlorideHCID 86683847Tert-butyl cis-2-(5-aminocarbonyl-6-chloro-3-fluoropyridin-2-ylamino)cyclohexylcarbamate

생성물 1

HCID 86683848Tert-butyl cis-2-(6-chloro-5-cyano-3-fluoropyridin-2-ylamino)cyclohexylcarbamate수율 76%

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

Trichloroacetyl chloride (0.55 ml) was added dropwise to a dichloromethane (17 ml) suspension containing tert-butyl cis-2-(5-aminocarbonyl-6-chloro-3-fluoropyridin-2-ylamino)cyclohexylcarbamate (1.74 g) and triethylamine (1.38 ml) under ice cooling, followed by stirring at room temperature for 1 hour. The solvent was distilled away under reduced pressure, and a saturated aqueous ammonium chloride solution and ethyl acetate were added. The organic layer was collected, washed with saturated saline, and dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:0 to 3:1), diisopropylether was added, solid matter was collected by filtration, and a white solid of tert-butyl cis-2-(6-chloro-5-cyano-3-fluoropyridin-2-ylamino)cyclohexylcarbamate (1.26 g) was thus obtained.

후처리

  1. distillationThe solvent was distilled away under reduced pressure
  2. additiona saturated aqueous ammonium chloride solution and ethyl acetate were added
  3. customThe organic layer was collected
  4. washwashed with saturated saline
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled away under reduced pressure
  7. customThe obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:0 to 3:1), diisopropylether
  8. additionwas added
  9. filtrationsolid matter was collected by filtration

출처 및 근거

ORD 기록
ord-153910a2126a4678b5bd7b09cdd3e97f
출처 데이터셋
uspto-grants-2014_08
특허 번호
US08809371B2

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