تفاعل #1731302

ord-2f37b32b656749a18672abd29581afa3

معادلة التفاعل

O=C(O)c1ccoc1
furan-3-carboxylic acid
On1nnc2ccccc21
HOBt
CCN=C=NCCCN(C)C.Cl
EDCI.HCl
N[C@@H]1CCCc2ccccc21
(R)-1,2,3,4-tetrahydronaphthalen-1-amine
O=C(N[C@@H]1CCCc2ccccc21)C1=CCOC1
(R)—N-(1,2,3,4-tetrahydronaphthalen-1-yl)-2,5-dihydrofuran-3-carboxamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe resulting solution was washed with saturated NaHCO3, H2O, brine
  2. 2
    تجفيفdried over MgSO4
  3. 3
    تركيزconcentrated in vacuo
  4. 4
    أخرىRecrystallization from EtOH/H2O

الإجراء التجريبي

To a solution of furan-3-carboxylic acid (100 mg, 0.68 mmol), HOBt (240 mg, 1.78 mmol) and EDCI.HCl (196 mg, 1.03 mmol) in CH2Cl2 (8 mL) and DMF (1.5 mL) at 0° C., was added (R)-1,2,3,4-tetrahydronaphthalen-1-amine (160 μL, 1.06 mmol). The reaction was stirred at rt for 24 h, after which CH2Cl2 was added. The resulting solution was washed with saturated NaHCO3, H2O, brine, dried over MgSO4 and concentrated in vacuo. Recrystallization from EtOH/H2O afforded (R)—N-(1,2,3,4-tetrahydronaphthalen-1-yl)-2,5-dihydrofuran-3-carboxamide. 1H NMR (500 MHz, CDCl3): δ 1.89 (m, 3H), 2.12 (m, 1H), 2.84 (m, 2H), 5.35 (m, 1H), 5.96 (br d, 1H, J=7.75 Hz), 6.59 (dd, 1H, J=1.90, 0.86 Hz), 7.13 (m, 1H), 7.19 (m, 2H), 7.32 (m, 1H), 7.43 (t, 1H, J=1.73 Hz), 7.93 (m, 1H). MS (M+H, 242).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08124121B2uspto-grants-2012_02