تفاعل #9271

ord-1c22368b0e704f58812f062c12896e4b

معادلة التفاعل

CCNC(=O)Nc1nc2ccc(C#N)cc2s1
N-(6-cyano-1,3-benzothiazol-2-yl)-N′-ethylurea
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[N]=[N+]=[N-]
azidotributylstannane
CCNC(=O)Nc1nc2ccc(-c3nn[nH]n3)cc2s1
N-Ethyl-N′-[6-(2H-1,2,3,4-tetraazol-5-yl)-1,3-benzothiazol-2-yl]urea

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthen refluxed for about 48–72 hours
  2. 2
    أخرىThe solvent was removed under reduced pressure
  3. 3
    workup.ADDITIONAbout 0.5 mL of dilute aqueous hydrochloric acid was added
  4. 4
    أخرىa white precipitate formed
  5. 5
    ترشيحthe precipitate was collected by filtration
  6. 6
    غسيلwashed with warm THF
  7. 7
    أخرىthen dried under vacuum
  8. 8
    أخرىLC/MS 1.37 min, 290 (M+1)

الإجراء التجريبي

About 30 mg N-(6-cyano-1,3-benzothiazol-2-yl)-N′-ethylurea was charged into about 5 mL dry tetrahydrofuran. Added about 2 g of azidotributylstannane then refluxed for about 48–72 hours. The solvent was removed under reduced pressure then the crude oil was taken up in dichloromethane. About 0.5 mL of dilute aqueous hydrochloric acid was added and a white precipitate formed. This was allowed to sit for about 30 minutes then the precipitate was collected by filtration, washed with warm THF then dried under vacuum. 1H NMR 1.10 (t, 3H), 3.2 (m, 2H), 6.76 (br s, 1H), 7.78 (d, 1H), 8.0 (d, 1H), 8.58 (s, 1H), 10.91 (s, 1H); LC/MS 1.37 min, 290 (M+1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091227B2uspto-grants-2006_08