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Hydrochloric Acid → HCID 86648485, 화합물

HRID 1424941
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HRID 1424941 반응식
[Cl:1][C:2]1[N:3]=[C:4]([C:9]([NH:11][C@H:12]2[CH2:17][CH2:16][N:15]([C:18](OC(C)(C)C)=O)[CH2:14][C@H:13]2[O:25][CH3:26])=[O:10])[NH:5][C:6]=1[CH2:7][CH3:8].Cl.C(OCC)(=O)C.C(N(C(C)C)CC)(C)C.ClC1[S:45][C:46]([CH3:54])=[C:47]([C:49]([O:51][CH2:52][CH3:53])=[O:50])[N:48]=1.Cl>CO>[Cl:1][C:2]1[N:3]=[C:4]([C:9]([NH:11][C@H:12]2[CH2:17][CH2:16][N:15]([C:18]3[S:45][C:46]([CH3:54])=[C:47]([C:49]([O:51][CH2:52][CH3:53])=[O:50])[N:48]=3)[CH2:14][C@H:13]2[O:25][CH3:26])=[O:10])[NH:5][C:6]=1[CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 81531DiisopropylethylamineHCID 21866389Hydrogen chloride-ethyl acetateHCID 53302340Ethyl 2-chloro-5-methyl-1,3-thiazole-4-carboxylateHCID 86648452tert-Butyl cis(+/-)-4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-methoxypiperidine-1-carboxylate

생성물 1

HCID 86648485
HCID 86648485, 화합물
수율 16%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

tert-Butyl cis(±)-4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-methoxypiperidine-1-carboxylate obtained by the method described in Example (1g) (80 mg, 0.21 mmol) was dissolved in methanol (1 mL). A 4 N hydrochloric acid/ethyl acetate solution (3 mL) was added, and the mixture was stirred at room temperature for one hour. Following concentration under reduced pressure, the residue was dissolved in DMF (2 mL). Diisopropylethylamine (0.16 mL, 0.92 mmol) and ethyl 2-chloro-5-methyl-1,3-thiazole-4-carboxylate obtained in Example (38a) (70 mg, 0.34 mmol) were added, and the mixture was stirred using a microwave reactor at 160° C. for three hours. Dilute hydrochloric acid was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with water, saturated aqueous sodium bicarbonate solution and brine, and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=4/1, 1/1, ethyl acetate) to obtain 15.3 mg of the title compound as a pale yellow solid (16%).

후처리

  1. concentrationconcentration under reduced pressure
  2. dissolutionthe residue was dissolved in DMF (2 mL)
  3. stirringthe mixture was stirred
  4. customat 160° C.
  5. customfor three hours
  6. extractionfollowed by extraction with ethyl acetate
  7. washThe organic layer was washed with water, saturated aqueous sodium bicarbonate solution and brine
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationconcentration under reduced pressure
  10. customthe residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=4/1, 1/1, ethyl acetate)

출처 및 근거

ORD 기록
ord-8586d4ea1de34ce2ab46c90d6d5952ce
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927588B2

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