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Hydrochloric Acid → methyl 1-amino-3-chloro-1H-pyrrole-2-carboxylate hydrochloride

HRID 1795941
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HRID 1795941 반응식
[H-].[Na+].[Cl:3][C:4]1[CH:8]=[CH:7][NH:6][C:5]=1[C:9]([O:11][CH3:12])=[O:10].Cl.C[N:15](C=O)C>[Li+].[Cl-].O1CCOCC1.CCOCC>[ClH:3].[NH2:15][N:6]1[CH:7]=[CH:8][C:4]([Cl:3])=[C:5]1[C:9]([O:11][CH3:12])=[O:10]
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참가 물질

8

반응물 4

HCID 313Hydrochloric AcidHCID 6228DimethylformamideHCID 24758Sodium hydrideHCID 5324605Methyl 3-chloro-1H-pyrrole-2-carboxylate

생성물 1

HCID 67017160methyl 1-amino-3-chloro-1H-pyrrole-2-carboxylate hydrochloride수율 99%

시약·촉매·용매 3

HCID 3283Diethyl Ether
용매
HCID 312751,4-Dioxane용매
HCID 433294Lithium Chloride용매

실험 절차

A mixture of sodium hydride (60%, 0.8 g, 20 mmol) and methyl 3-chloro-1H-pyrrole-2-carboxylate (Tetrahedron, 1999, 55, 4133–4152; 2.5 g, 15.7 mmol) in DMF (10 mL) at 0° C. was stirred for 25 min, then was added 2,4-dinitrophenolamine (Tetrahedron Lett. 1968, 16, 1909–1910 and J. Heterocyclic Chem. 1967, 413, 3.80 g, 19.1 mmol) and the reaction mixture was stirred at 0–5° C. for 2.5 h. The mixture was diluted with 10% aqueous LiCl solution and the product was extracted with EtOAc (3×100 mL). The EtOAc solution was washed with 10% LiCl solution (2×80 mL), brine (80 mL), dried over MgSO4 and concentrated in vacuo to give the crude product as a brown oil. The crude product was treated with 4 N HCl in dioxane (2 mL) in Et2O (60 mL). The precipitated solid was collected, washed with Et2O and dried in vacuo to obtain the title compound (3.30 g, 99%): 1H NMR (DMSO-d6) δ 7.17 (d, 1H, J=2.2 Hz), 6.68 (d, 1H, J=2.2 Hz), 3.74 (s, 3H).

후처리

  1. stirringthe reaction mixture was stirred at 0–5° C. for 2.5 h
  2. extractionthe product was extracted with EtOAc (3×100 mL)
  3. washThe EtOAc solution was washed with 10% LiCl solution (2×80 mL), brine (80 mL)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customto give the crude product as a brown oil
  7. customThe precipitated solid was collected
  8. washwashed with Et2O
  9. customdried in vacuo

출처 및 근거

ORD 기록
ord-d52e4c616db447058f6640dc3a1198f3
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07030118B2

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