Reacción #631985

ord-951c92fef45949fcaa40b80a54585bfd

Ecuación de reacción

CCc1c(C(=O)NNC(C=C(C)C(C)(C)C)C(C)(C)C)ccc2c1OCCO2
5-Ethyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid N′-(1-tert-butyl-3,4,4-trimethyl-pent-2-enyl)-hydrazide
COc1cc(C(=O)Cl)cc(OC)c1C
3,5-dimethoxy-4-methylbenzoyl chloride
O=C([O-])[O-].[K+].[K+]
K2CO3
CCc1c(C(=O)NN(C(=O)c2cc(OC)c(C)c(OC)c2)C(C=C(C)C(C)(C)C)C(C)(C)C)ccc2c1OCCO2
3,5-dimethoxy-4-methyl-benzoic acid N-(1-tert-butyl-3,4,4-trimethyl-pent-2-enyl)-N′-(5-ethyl-2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)-hydrazide
Rendimiento 38.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe phases were separated
  2. 2
    workup.ADDITIONadding additional CH2Cl2 and/or water
  3. 3
    SecadoThe CH2Cl2 layer was dried
  4. 4
    Otrosolvent was removed in vacuo
  5. 5
    Otroto provide 210 mg of crude product
  6. 6
    OtroThis material was purified by silica gel column chromatography
  7. 7
    Lavadoeluting with a step gradient of 10-25% ethyl acetate in hexane

Procedimiento

5-Ethyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid N′-(1-tert-butyl-3,4,4-trimethyl-pent-2-enyl)-hydrazide (150 mg, 0.39 mmol) and 3,5-dimethoxy-4-methylbenzoyl chloride (83 mg, 0.39 mmol) were dissolved in 5 mL CH2Cl2. 5 mL of 25% K2CO3 were added, and the reaction mixture was stirred at room temperature overnight. The reaction was monitored by TLC. The phases were separated, adding additional CH2Cl2 and/or water as needed to aid manipulation. The CH2Cl2 layer was dried and solvent was removed in vacuo to provide 210 mg of crude product. This material was purified by silica gel column chromatography, eluting with a step gradient of 10-25% ethyl acetate in hexane to yield 3,5-dimethoxy-4-methyl-benzoic acid N-(1-tert-butyl-3,4,4-trimethyl-pent-2-enyl)-N′-(5-ethyl-2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)-hydrazide RG115898 (83 mg, Rf=0.19 in 25% ethyl acetate in n-hexane, yield 38%). 1H NMR (400 MHz, DMSO-d6) δ (ppm): 10.19 (s, 1H), 6.75 (d, J=8.0 Hz, 1), 6.69 (s, 2H), 6.61 (d, J=8.0 Hz, 1H), 5.43 (d, J=10.0 Hz, 1H), 5.41 (d, 14.4 Hz, 1H), 4.30-4.20 (m, 4H), 3.80 (s, 6H), 2.21-2.15 (m, 1H), 2.01 (s, 3H), 1.81 (m, 1H), 1.76-1.64 (m, 1H), 1.06 (s, 9H), 1.00 (s, 9H), 0.70 (t, J=7.6 Hz, 3H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07935510B2uspto-grants-2011_05