반응 #710549

ord-a812c5ac6e23473ca30dbbb0cd49383e

반응 방정식

O=C([O-])O.[Na+]
sodium bicarbonate
CC(C)CC(N)C1(c2ccc(Cl)cc2)CCC1
cyclobutane amine
CC(C)CC(N)C1(c2ccc(Cl)cc2)CCC1
1-[1-(4-Chlorophenyl)cyclobutyl]-3-methylbutan-1-amine
CCOC(=O)C=O
ethyl glyoxylate
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
sodium triacetoxyborohydride
CCOC(=O)CNC(CC(C)C)C1(c2ccc(Cl)cc2)CCC1
54a
CCOC(=O)CNC(CC(C)C)C1(c2ccc(Cl)cc2)CCC1
Ethyl 2-(1-(1-(4-chlorophenyl)cyclobutyl)-3-methylbutylamino]acetate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted with ethyl acetate (50 mL×3)
  2. 2
    추출The combined extract
  3. 3
    세척was washed with water (50 mL)
  4. 4
    건조dried over sodium sulfate (Na2SO4)
  5. 5
    기타evaporated
  6. 6
    기타The residue was purified by silica gel column chromatography

실험 절차

To a stirred solution of cyclobutane amine 52a (0.68 g, 0.0027 mole) and ethyl glyoxylate (50% solution in toluene) (1.02 g, 0.01 mole) in 20 mL of a mixture of solvents DMF and acetic acid (ratio, 99:1) was added sodium triacetoxyborohydride (2.11 g, 0.01 mole) portion-wise over a period of 15 minutes at room temperature. The resulting mixture was stirred for 8 hours at room temperature and the progress of the reaction was monitored by TLC. The reaction mixture was poured in to saturated sodium bicarbonate solution (50 mL) and extracted with ethyl acetate (50 mL×3). The combined extract was washed with water (50 mL), dried over sodium sulfate (Na2SO4) and evaporated. The residue was purified by silica gel column chromatography using 0-50% gradient of ethyl acetate and hexane as eluents to give pure 54a as colorless liquid in 45% (0.41 g) yield. The 1H NMR and mass spectral data are identical to the compound synthesized using the protocol described for the synthesis of 54a-e (Example 3, Scheme 7).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09302981B2uspto-grants-2016_04