تفاعل #2175467

ord-48109129a7ec4dbdb682068e71398eba

معادلة التفاعل

O=C([O-])O.[Na+]
NaHCO3
C[C@H](COC(=O)[C@@H](N)Cc1ccc(O)c(O)c1)OC(=O)c1ccccc1.Cl
hydrochloride salt
C[C@H](COC(=O)[C@@H](N)Cc1ccc(O)c(O)c1)OC(=O)c1ccccc1.Cl
(2R)-2-Phenylcarbonyloxypropyl (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoate hydrochloride
CS(=O)(=O)O
Methanesulfonic acid
CCOC(C)=O
ethyl acetate
CS(=O)(=O)O
methanesulfonic acid
CS(=O)(=O)O.C[C@H](COC(=O)[C@@H](N)Cc1ccc(O)c(O)c1)OC(=O)c1ccccc1
mesylate salt
المردود 99.3%
CS(=O)(=O)O.C[C@H](COC(=O)[C@@H](N)Cc1ccc(O)c(O)c1)OC(=O)c1ccccc1
(2R)-2-Phenylcarbonyloxypropyl (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoate mesylate
المردود 99.3%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصThe resulting aqueous suspension was extracted with ethyl acetate (EtOAc) (2×400 mL)
  2. 2
    استخلاصThe combined EtOAc extract
  3. 3
    غسيلwas washed with water
  4. 4
    تجفيفbrine, and dried through MgSO4
  5. 5
    أخرىWhite precipitate
  6. 6
    أخرىformed as
  7. 7
    workup.STIRRINGThe suspension was stirred for another 30 min
  8. 8
    ترشيحfiltered
  9. 9
    غسيلThe filter cake was washed three times with ethyl acetate (EtOAc) and vacuum
  10. 10
    أخرىdried overnight

الإجراء التجريبي

A solution of NaHCO3 (9.87 g, 117.5 mmol) in water (80 mL) was slowly added to a solution of hydrochloride salt 1d (31.0 g, 78.3 mmol) in water (300 mL). The resulting aqueous suspension was extracted with ethyl acetate (EtOAc) (2×400 mL). The combined EtOAc extract was washed with water, then brine, and dried through MgSO4. Methanesulfonic acid (6.04 mL, 93.12 mmol) was slowly added to the ethyl acetate (EtOAc) solution while stirred. White precipitate formed as soon as the addition of methanesulfonic acid was complete. The suspension was stirred for another 30 min and then filtered. The filter cake was washed three times with ethyl acetate (EtOAc) and vacuum dried overnight to afford 35.4 g (quantitative yield) of anhydrous mesylate salt 1 as a white solid. 1H NMR (400 MHz, CD3OD): δ 1.40 (d, J=6.4 Hz, 3H), 2.70 (s, 3H), 2.98 (dd, J=7.8, 14.6 Hz, 1H), 3.10 (dd, J=5.6, 14.4 Hz, 1H), 4.24 (dd, J=5.8, 7.8 Hz, 1H), 4.38 (dd, J=6.8, 12.0 Hz, 1H), 4.52 (dd, J=3.4, 11.8 Hz, 1H), 5.40 (dp, J=3.2, 6.4 Hz, 1H), 6.52 (dd, J=2.2, 8.2 Hz, 1H), 6.67 (d, J=2.2 Hz, 1H), 6.69 (d, J=8.0 Hz, 1H), 7.47 (t, J=7.6 Hz, 2H), 7.60 (br t, J=7.4 Hz, 1H), 8.01 (d, J=7.6 Hz, 2H). MS (ESI) m/z 360.07 (M+H)+ and 358.01 (M−H)−.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08435562B2uspto-grants-2013_05