Reaktion #9705

Reaktionsgleichung

HCl

methyl (1R,2R)-2-[(4′-amino-1,1′-biphenyl-4-yl)carbonyl]cyclopentane-carboxylate

2-chloro-6-(trifluoromethyl)-1,3-benzothiazole

→

title compound

Ausbeute 13.0%

(1R,2R)-2-[(4′-{[6-(Trifluoromethyl)-1,3-benzothiazol-2-yl]amino}-1,1′-biphenyl-4-yl)carbonyl]cyclopentanecarboxylic acid

Ausbeute 13.0%

Lösungsmittel

n-butanol

dioxane

diethyl ether

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenThe reaction mixture was concentrated under reduced pressure
2. 2
   Sonstigepurified by flash chromatography on silica gel
3. 3
   Wascheneluting with a gradient from 9:1 to 3:2 hexanes/ethyl acetate
4. 4
   SonstigeThe product obtained
5. 5
   Filtrationthe resulting solid was collected by filtration
6. 6
   Waschenwashed with additional diethyl ether and hexanes
7. 7
   SonstigeLC-MS m/z 567.3 (MH+), 4.67 min
8. 8
   workup.ADDITIONThe off-white solid was diluted with methanol (2 mL) and tetrahydrofuran (2 mL)
9. 9
   workup.ADDITIONtreated with 2 M aqueous sodium hydroxide solution (2 mL)
10. 10
    workup.ADDITIONThe mixture was acidified by the addition of an excess of 2 M aqueous hydrochloric acid solution
11. 11
    ExtraktionThe acidic solution was extracted with ethyl acetate
12. 12
    Trocknendried (MgSO4)
13. 13
    Einengenconcentrated under reduced pressure
14. 14
    Sonstigethe resulting solids were removed by filtration
15. 15
    Einengenwas concentrated under reduced pressure

Vorschrift

A mixture of methyl (1R,2R)-2-[(4′-amino-1,1′-biphenyl-4-yl)carbonyl]cyclopentane-carboxylate (150 mg, 0.464 mmol) and 2-chloro-6-(trifluoromethyl)-1,3-benzothiazole(132 mg, 0.557 mmol) was diluted with n-butanol (3 mL) and treated with a catalytic amount of 4 M HCl in dioxane. The suspension was heated at 90° C. overnight. The reaction mixture was concentrated under reduced pressure and purified by flash chromatography on silica gel, eluting with a gradient from 9:1 to 3:2 hexanes/ethyl acetate. The product obtained was suspended in diethyl ether, and the resulting solid was collected by filtration and washed with additional diethyl ether and hexanes. LC-MS for the n-butyl ester: LC-MS m/z 567.3 (MH+), 4.67 min; 1H NMR (300 MHz, CDCl3) δ 8.14–8.10 (m, 3 H), 7.80–7.71 (m, 6 H), 7.62 (d, 2 H), 4.17–4.13 (m, 1 H), 4.09–4.04 (m,2 H), 3.51–3.41 (m, 1 H), 2.21–2.13 (m, 2 H), 1.97–1.90 (m, 1 H), 1.81–1.78 (m, 3 H), 1.58–1.51 (m, 2 H), 1.35–1.28 (m, 2 H),1.23–1.18 (t, 3 H), 0.88 (t, 2 H). The off-white solid was diluted with methanol (2 mL) and tetrahydrofuran (2 mL) and treated with 2 M aqueous sodium hydroxide solution (2 mL). The solution was stirred overnight at rt. The mixture was acidified by the addition of an excess of 2 M aqueous hydrochloric acid solution. The acidic solution was extracted with ethyl acetate. The organic phases were combined, dried (MgSO4), and concentrated under reduced pressure. The residue was suspended in methanol and the resulting solids were removed by filtration. The filtrate, which contained the product, was concentrated under reduced pressure to provide the title compound as a pale orange solid (30 mg, 13% overall yield). 1H NMR (tetrahydrofuran-d8) δ 10.85 (s, 1 H), 8.11–8.07 (m, 3 H), 7.96–7.91 (m, 2 H), 7.79–7.71 (m, 5 H), 7.63–7.59 (dd, 1 H), 4.18 (q, 1 H), 3.37 (q, 1 H), 2.2–1.77 (m, 6 H); LC-MS m/z 511.3 (MH+), retention time 4.27 minutes.

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