تفاعل #1929070

ord-164619ac57764371a9d762a087793152

معادلة التفاعل

CCN(CC)CC
triethylamine
COC(=O)C1(N)CCC(F)(F)CC1.Cl
compound
COC(=O)C1(N)CCC(F)(F)CC1.Cl
Methyl 1-amino-4,4-difluorocyclohexanecarboxylate hydrochloride
CCN(CC)CC
triethylamine
O=P(Cl)(Cl)Cl
phosphorus oxychloride
Cc1ccc(-c2ccc(F)cc2)cc1CC(=O)O
(4′-fluoro-4-methylbiphenyl-3-yl)acetic acid
COC(=O)C1(NC(=O)Cc2cc(-c3ccc(F)cc3)ccc2C)CCC(F)(F)CC1
Methyl 4,4-difluoro-1-{[(4′-fluoro-4-methylbiphenyl-3-yl)acetyl]amino}cyclohexanecarboxylate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITAfter 15 min
  2. 2
    workup.STIRRINGthe mixture was stirred
  3. 3
    درجة الحرارةunder reflux for 30 min
  4. 4
    تركيزThe mixture was concentrated under reduced pressure
  5. 5
    أخرىthe residue was purified by means of flash chromatography on silica gel using the mobile phase n-hexane/ethyl acetate 1:1

الإجراء التجريبي

2.53 g (11 mmol) of the compound from Example 4A were initially charged in 50 ml of absolute tetrahydrofuran (THF). At 20° C., 3.07 ml of triethylamine were added dropwise, the mixture was stirred for 5 min and 2.44 g (10 mmol) of (4′-fluoro-4-methylbiphenyl-3-yl)acetic acid were added. After 15 min, a further 2.3 ml of triethylamine were added, followed immediately by the dropwise addition of 0.58 ml (6.2 mmol) of phosphorus oxychloride, and the mixture was stirred under reflux for 30 min. The mixture was concentrated under reduced pressure and the residue was purified by means of flash chromatography on silica gel using the mobile phase n-hexane/ethyl acetate 1:1. This gave 2.84 g (60% of theory) of the title compound of melting point 187° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08946124B2uspto-grants-2015_02