تفاعل #531859

ord-b2099384486847fa9b7a00161b0e5074

معادلة التفاعل

O=C(O)CCCCCCCBr
8-bromooctanoic acid
CCO
ethanol
CCN=C=NCCCN(C)C
EDCI
CCOC(=O)CCCCCCCBr
8-bromooctanoic acid ethyl ester
المردود 76.1%

الكواشف

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلthe reaction mixture was washed with 1 N NaOH aqueous solution (15 mL) and water (30 mL)
  2. 2
    تجفيفthe organic layer was dried over Na2SO4
  3. 3
    أخرىevaporated

الإجراء التجريبي

To a solution of 8-bromooctanoic acid (0.20 g, 0.89 mmol), DMAP (0.12 g, 0.99 mmol), and ethanol (0.05 g, 0.99 mmol) in methylene chloride (20 mL) was added EDCI (0.19 g, 0.99 mmol) at room temperature. After stirring for 12 h, the reaction mixture was washed with 1 N NaOH aqueous solution (15 mL) and water (30 mL), and the organic layer was dried over Na2SO4 and evaporated to give 8-bromooctanoic acid ethyl ester (0.17 g, 75%). This bromide reacted with 4-(3-adamantan-1-yl-ureido)butyric acid 822 in the same manner as that used for the preparation of 883 to provide 879 (0.19 g, 65%) as a solid: 1H NMR (CDCl3) 1.26 (3H, t, J=6.9 Hz), 1.32-1.35 (6H, m), 1.59-1.66 (10H, m), 1.82 (2H, quint, J=6.9 Hz), 1.94-1.97 (6H, m), 2.05-2.07 (3H, m), 2.28 (2H, t, J=6.9 Hz), 2.36 (2H, t, J=6.9 Hz), 3.16 (2H, q, J=6.9 Hz), 4.05-4.14 (5H, m), 4.31 (1H, s); LC-MS (ESI) m/z calcd for C25H42N2O5 [M+H]+ 451.31. found [M+H]+ 451.20; mp 58-59 C. Anal. (C25H42N2O5) C, H, N.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08476043B2uspto-grants-2013_07