تفاعل #73901

ord-3a8f14a95948498ca5cf913034bba66f

معادلة التفاعل

c1ccc2c(c1)N=N[NH2+]2
1H-Benzotriazolium
F[B-](F)(F)F
tetrafluoroborate
CNC
dimethylamine
COC(=O)[C@H](CC(C)C)N[C@@H](C(=O)Nc1ccccc1O)c1ccc2occc2c1
methyl N-{(1R)-1-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinate
S=C(n1ccnc1)n1ccnc1
1,1′-thiocarbonyldiimidazole
COC(=O)[C@H](CC(C)C)NC(C(=O)N(C)C)c1ccc2occc2c1
methyl N-[1-(benzofuran-5-yl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate
المردود 40.5%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe reaction mixture was stirred for a further 18 hours
  2. 2
    غسيلeluting with a gradient (3:1 to 1:2 cyclohexane:ethyl acetate)
  3. 3
    أخرىevaporated

الإجراء التجريبي

A solution of methyl N-{(1R)-1-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinate (410 mg) and 1,1′-thiocarbonyldiimidazole (196 mg) in dichloromethane (5 ml) was left to stand for 18 hours. Water (20 l) was added to the reaction mixture and this was then stirred rapidly for 30 minutes. After this, 1H-Benzotriazolium, 1-[bis(dimethylamino)methylene]-, tetrafluoroborate (1-), 3-oxide (TBTU, 710 mg) and a solution of dimethylamine in tetrahydrofuran (3 ml of 2M solution) were added. The reaction mixture was stirred for a further 18 hours and was then passed down an SPE (5 g, silica) eluting with a gradient (3:1 to 1:2 cyclohexane:ethyl acetate). The required fractions were combined and evaporated to furnish methyl N-[1-(benzofuran-5-yl)-2-(dimethylamino)-2-oxoethyl]-L-leucinate (140 mg).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08541579B2uspto-grants-2013_09