Water → HCID 90102988, compound

HRID 1051210Notes

Reaction equation

HRID 1051210 reaction equation
C(OC([C:8]1[CH:13]=[CH:12][C:11]([CH2:14][CH:15](OC(=O)C(F)(F)F)[C:16]2[C:17]([O:23][CH3:24])=[N:18][CH:19]=[CH:20][C:21]=2[I:22])=[C:10]([N+:32]([O-:34])=[O:33])[C:9]=1N)=O)(C)(C)C.[OH2:36]>C1COCC1>[C:11]([O:36][C:17](=[O:23])[NH:18][C:8]1[CH:13]=[CH:12][C:11](/[CH:14]=[CH:15]/[C:16]2[C:17]([O:23][CH3:24])=[N:18][CH:19]=[CH:20][C:21]=2[I:22])=[C:10]([N+:32]([O-:34])=[O:33])[CH:9]=1)([CH3:14])([CH3:12])[CH3:10]

Participants

4

Conditions

Temperature
70 °C

Procedure

A solution of crude trifluoro-acetic acid 2-(4-tert-butoxycarbonyl-amino-2-nitro-phenyl)-1-(4-iodo-2-methoxy-pyridin-3-yl)-ethyl ester (crude 1.88 g, 3.08 mmol) in THF (10 mL) was added 8-diazabicyclo[5.4.0]undec-7-ene (1.33 g, 8.74 mmol) at 25° C. The reaction was allowed to stir at 70° C. for 3 hours. The reaction mixture was cooled to 25° C., and poured into water. The aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried over magnesium sulfate. Filtration followed by concentration in vacuo gave a brown solid. Flash chromatography (80/20 hexanes/ethyl acetate) afforded {4-[(E)-2-(4-iodo-2-methoxy-pyridin-3-yl)-vinyl]-3-nitro-phenyl}-carbamic acid tert-butyl ester (850 mg, 55%) as an oil. MH+ 497.9.

Workup

  1. temperatureThe reaction mixture was cooled to 25° C.
  2. extractionThe aqueous phase was extracted three times with ethyl acetate
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationFiltration
  6. concentrationfollowed by concentration in vacuo
  7. customgave a brown solid

Sources & evidence

ORD record
ord-fddb135bbdc04f5796bdb569a09939ce
Source dataset
uspto-grants-2016_07
Patent number
US09388166B2

Reaction notes

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