تفاعل #48349

ord-f7d1df756e7e40a0881c4558b51835be

معادلة التفاعل

O=C([O-])O.[Na+]
sodium bicarbonate
O=C(Cl)Cl
Phosgene
O=c1[nH]c2[nH+]cccc2n1C1CC[NH2+]CC1.[Cl-].[Cl-]
2-oxo-1-piperidinium-4-yl-2,3-dihydro-1H-imidazo[4,5-b]pyridin-4-ium dichloride
Cc1cccc(C)n1
2,6-lutidine
O=C(Cl)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
title compound
المردود 49.9%
O=C(Cl)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
4-(2-Oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-1-yl)piperidine-1-carbonyl chloride
المردود 49.9%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate
  2. 2
    غسيلThe organic layer was washed with water (2×), saturated brine
  3. 3
    تجفيفdried over magnesium sulfate
  4. 4
    ترشيحfiltered
  5. 5
    تركيزconcentrated
  6. 6
    workup.ADDITIONDichloromethane (10 mL) was added
  7. 7
    ترشيحthe mixture was filtered

الإجراء التجريبي

Phosgene (20% wt. in toluene; 1.8 mL, 3.43 mmol) was added to a suspension of 2-oxo-1-piperidinium-4-yl-2,3-dihydro-1H-imidazo[4,5-b]pyridin-4-ium dichloride (100 mg, 0.343 mmol) and 2,6-lutidine (0.50 mL, 4.293 mmol) in dichloromethane (5 mL) at 0° C. After 2 h, the solution was added to saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The organic layer was washed with water (2×), saturated brine, dried over magnesium sulfate, filtered and concentrated. Dichloromethane (10 mL) was added, and the mixture was filtered to give the title compound as a solid (48 mg). MS 281 (M+1). 1H NMR (500 MHz, (CD3)2SO) δ 11.58 (s, 1H), 7.90 (d, J=5.1 Hz, 1H), 7.67 (d, J=7.6 Hz, 1H), 7.01-6.99 (m, 1H), 4.52-4.46 (m, 1H), 4.31-4.23 (m, 2H), 3.38-3.33 (m, 1H), 3.19-3.14 (m, 1H), 2.32-2.24 (m, 2H), 1.84-1.81 (m, 2H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745427B2uspto-grants-2010_06