تفاعل #326955

ord-497ddc527a5543ecacbd5f8fdb4364ff

معادلة التفاعل

NC(=O)C(N)c1ccccc1
D-Phenylglycine amide
O=S1(=O)CCCO1
1,3-propanesultone
NC(=O)[C@@H](NCCCS(=O)(=O)O)c1ccccc1
title compound
المردود 38.9%
NC(=O)[C@@H](NCCCS(=O)(=O)O)c1ccccc1
3-{[(1S)-2-amino-2-oxo-1-phenylethyl]amino}-1-propanesulfonic acid
المردود 38.9%

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux for 2 hours
  2. 2
    ترشيحThe solid was collected by filtration
  3. 3
    غسيلwashed with acetone (2×20 mL)
  4. 4
    workup.DISSOLUTIONThe solid was dissolved in 50% water/EtOH mL)
  5. 5
    workup.ADDITIONDowex Marathon C ion exchange resin (strongly acidic) was added to the solution
  6. 6
    workup.STIRRINGThe suspension was stirred for 15 minutes before the resin
  7. 7
    أخرىwas removed by filtration
  8. 8
    أخرىThe filtrate was evaporated under reduced pressure
  9. 9
    ترشيحfiltered
  10. 10
    أخرىdried in the vacuum oven (50° C.)

الإجراء التجريبي

To a solution of D-Phenylglycine amide (850 mg, 7.5 mmol) in tetrahydrofuran (10 mL) and 1,4-dioxane (4 mL) was added 1,3-propanesultone (818 mg, 6.8 mmol). The solution stirred at reflux for 2 hours. The reaction was cooled to room temperature. The solid was collected by filtration and washed with acetone (2×20 mL). The solid was dissolved in 50% water/EtOH mL). Dowex Marathon C ion exchange resin (strongly acidic) was added to the solution. The suspension was stirred for 15 minutes before the resin was removed by filtration. The filtrate was evaporated under reduced pressure. The solid was suspended in acetone (50 mL), filtered and dried in the vacuum oven (50° C.), affording the title compound (720 mg, 34%). 1H NMR (D2O, 500 MHz) δ ppm 7.38 (m, 5H), 4.92, (s, 1H), 3.00 (m, 1H), 2.90 (m, 1H), 2.78 (m, 2H), 1.97 (m, 2H). 13C (D2O, 125 MHz) δ ppm 170.14, 130.95, 130.24, 129.94, 128.74, 63.40, 47.99, 44.92, 21.27. [α]D=+106° (c=0.0016 in water), ES-MS 273 (M+1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08642801B2uspto-grants-2014_02