تفاعل #328502

ord-4e6e9f6096b342cf9a5d924216b1e160

معادلة التفاعل

O
water
COc1ccc2cc([C@H](C)C(=O)O)ccc2c1
(S)-2-(6-methoxy-naphthalen-2-yl)-propionic acid
CCN=C=NCCCN(C)C.Cl
1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride
OC(Cc1c(Cl)cncc1Cl)c1ccc(OC(F)F)c(OCC2CC2)c1
Compound ( 3 )
OC(Cc1c(Cl)cncc1Cl)c1ccc(OC(F)F)c(OCC2CC2)c1
1-(3-Cyclopropylmethoxy-4-difluoromethoxy-phenyl)-2-(3,5-dichloro-pyridin-4-yl)-ethanol
COc1ccc2cc(C(C)C(=O)OC(Cc3c(Cl)cncc3Cl)c3ccc(OC(F)F)c(OCC4CC4)c3)ccc2c1
oil
المردود 92.9%
COc1ccc2cc(C(C)C(=O)OC(Cc3c(Cl)cncc3Cl)c3ccc(OC(F)F)c(OCC4CC4)c3)ccc2c1
2-(6-Methoxy-naphthalen-2-yl)-propionic acid 1-(3-cyclopropylmethoxy-4-difluoromethoxy-phenyl)-2-(3,5-dichloro-pyridin-4-yl)-ethyl ester
المردود 92.9%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصThe mixture was extracted with EtOAc (500 ml×2)
  2. 2
    تجفيفthe combined organic layers are dried over sodium sulphate
  3. 3
    أخرىthe solvent was removed by evaporation under reduced pressure

الإجراء التجريبي

Compound (3) (12.0 g) was dissolved in DMF (100 ml) then (S)-2-(6-methoxy-naphthalen-2-yl)-propionic acid (7.5 g), 4-dimethylaminopyridine (3.6 g), and 1-ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride (5.7 g) was added. After stirring at rt for 4 hours, water (1000 ml) is added. The mixture was extracted with EtOAc (500 ml×2), the combined organic layers are dried over sodium sulphate, and the solvent was removed by evaporation under reduced pressure to afford 17.0 g of an oil which is crystallized from EtOH thus obtaining 11.5 g of the title compound as mixture of diastereomers (11) and (13),

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08648204B2uspto-grants-2014_02