تفاعل #1929069

ord-5094d5c601ea4f4f96159411079a96ce

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(Cl)cc2)cc1CC(=O)O
(4′-chloro-4-methylbiphenyl-3-yl)acetic acid
COC(=O)C1(NC(=O)Cc2cc(-c3ccc(Cl)cc3)ccc2C)CCC(F)(F)CC1
Methyl 1-{[(4′-chloro-4-methylbiphenyl-3-yl)acetyl]amino}-4,4-difluorocyclohexanecarboxylate

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). 3.07 ml of triethylamine were added dropwise at 20° C., the mixture was stirred for 5 min, and 2.61 g (10 mmol) of (4′-chloro-4-methylbiphenyl-3-yl)acetic acid (EP 2029531 A1 and US 2009/298828 A1) 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 3.6 g (73% of theory) of the title compound of melting point 186° C.

المصدر

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