تفاعل #2178795

ord-6680b7f8ed3545488ba8450c339e8c12

معادلة التفاعل

COC(=O)c1cc(N)cs1
Methyl 4-aminothiophene-2-carboxylate
O=C(O)c1cc(F)ccn1
4-fluoropicolinic acid
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
CN1CCOCC1
N-methylmorpholine
COC(=O)c1cc(NC(=O)c2cc(F)ccn2)cs1
methyl 4-(4-fluoropicolinamido)thiophene-2-carboxylate
المردود 56.0%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwarmed to room temperature
  2. 2
    workup.STIRRINGstirred for an additional 2 hours
  3. 3
    أخرىThe solvent was removed under reduced pressure
  4. 4
    أخرىthe solids were isolated by filtration
  5. 5
    غسيلwashed with water, acetonitrile
  6. 6
    أخرىdried

الإجراء التجريبي

A solution of 4-fluoropicolinic acid (1.0 g, 6.4 mmol), HATU (2.9 g, 7.6 mmol), and N-methylmorpholine (0.84 mL, 7.6 mmol) in N,N-dimethylformamide (12 mL) was stirred at 0° C. for 30 minutes. Methyl 4-aminothiophene-2-carboxylate (990 mg, 7.0 mmol) was added, the reaction was stirred for 30 minutes at 0° C., then warmed to room temperature, and stirred for an additional 2 hours. The solvent was removed under reduced pressure, the residue was suspended in acetonitrile/H2O (1:1) and the solids were isolated by filtration, washed with water, acetonitrile, then dried to afford methyl 4-(4-fluoropicolinamido)thiophene-2-carboxylate as a white powder (1.0 g, 56% yield). M+1=281.1.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08440665B2uspto-grants-2013_05