반응 #10052

ord-3def3715b4dc4e31a7dc2480193bc963

반응 방정식

CCN(CC)CC
Triethylamine
COC(=O)c1cccc(CN)c1C(=O)OC.Cl
methyl-3-(aminomethyl)-2-(methoxycarbonyl)benzoate hydrochloride
O=C(Cl)OCc1ccccc1
Benzyl chloroformate
COC(=O)c1cccc(CNC(=O)OCc2ccccc2)c1C(=O)OC
product
수율 76.0%
COC(=O)c1cccc(CNC(=O)OCc2ccccc2)c1C(=O)OC
Methyl-3-[(benzyloxycarbonylamino)methyl]-2-(methoxycarbonyl)benzoate
수율 76.0%

반응 조건

온도
4°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타between 4–7° C
  2. 2
    workup.ADDITIONAfter the addition
  3. 3
    온도warmed to room temperature for 4 hours
  4. 4
    세척The mixture was washed with water (2×30 ml), brine (30 ml)
  5. 5
    기타dried
  6. 6
    기타Solvent was removed
  7. 7
    기타the residue was purified by chromatography (dichloromethane/ethyl acetate 95 to 5)

실험 절차

Triethylamine (1.87 g, 18.5 mmol) was added to a stirred suspension of methyl-3-(aminomethyl)-2-(methoxycarbonyl)benzoate hydrochloride (2.0 g, 8 mmol) in dichloromethane (30 ml). The mixture was cooled in an ice bath to 4° C. Benzyl chloroformate (1.66 g, 10 mmol) was added slowly keeping the temperature between 4–7° C. After the addition was complete, the cooled mixture was stirred an additional 30 minutes and then warmed to room temperature for 4 hours. The mixture was washed with water (2×30 ml), brine (30 ml) and dried. Solvent was removed and the residue was purified by chromatography (dichloromethane/ethyl acetate 95 to 5) to give 2.1 g (76%) of the product as a solid; 1H NMR (CDCl3) δ 7.87 (d, J=7.8 Hz, 1H), 7.63 (d, J=7.6 Hz, 1H), 7.46 (t, J=7.7 Hz, 1H), 7.36–7.26 (m, 5H), 5.41 (b, 1H), 5.09 (s, 2H), 4.36 (d, J=6.3 Hz, 2H), 3.91 (s, 3H), 3.88 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091353B2uspto-grants-2006_08