반응 #1074567

ord-42be9a9624214975863e00402913c28e

반응 방정식

O=C1COCC(=O)C1
product
O=C1COCC(=O)C1
2H-pyran-3,5(4H,6H)-dione
Cc1ccc(C=O)cc1I
product
Cc1ccc(C=O)cc1I
3-iodo-4-methylbenzaldehyde
COC(=O)/C=C(/C)N
methyl 3-aminocrotonate
COC(=O)C1=C(C)NC2=C(C(=O)COC2)C1c1ccc(C)c(I)c1
title compound
수율 45.5%
COC(=O)C1=C(C)NC2=C(C(=O)COC2)C1c1ccc(C)c(I)c1
methyl 4-(3-iodo-4-methylphenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylate
수율 45.5%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과the mixture was filtered
  2. 2
    세척the filter cake washed with methanol
  3. 3
    기타dried

실험 절차

The product from Example 1C (0.34 g, 3.0 mmol), the product from Example 3A (0.74 g, 3.0 mmol) and methyl 3-aminocrotonate (0.35 g, 3.0 mmol) in methanol (8 mL) were heated to 80° C. in a sealed tube for 60 hours. After cooling to ambient temperature, the mixture was filtered and the filter cake washed with methanol and dried to provide the title compound (0.60 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06632418B2uspto-grants-2003_10