تفاعل #1121781

ord-c64fe8931435479e8b0e4572e241bf33

معادلة التفاعل

COc1ccc(Sc2[nH]c(-c3ccccc3)cn3c(=O)c(Cc4ccccc4)nc2-3)cc1
231
COc1ccc(Sc2[nH]c(-c3ccccc3)cn3c(=O)c(Cc4ccccc4)nc2-3)cc1
2-Benzyl-8-(4-methoxyphenylthio)-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one
CC(=O)Cl
acetyl chloride
COc1ccc(Sc2nc(-c3ccccc3)cn3c(OC(C)=O)c(Cc4ccccc4)nc23)cc1
25a
المردود 66.0%
COc1ccc(Sc2nc(-c3ccccc3)cn3c(OC(C)=O)c(Cc4ccccc4)nc23)cc1
2-Benzyl-8-(4-methoxyphenylthio)-6-phenylimidazo[1,2-a]pyrazin-3-yl acetate
المردود 66.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThen the solution was washed with water
  2. 2
    تجفيفthe organic layer was dried over Na2SO4
  3. 3
    ترشيحfiltered
  4. 4
    أخرىthe solvent removed under reduced pressure

الإجراء التجريبي

To a solution of 231 (25 mg, 0.06 mmol) in 4 mL of dichloromethane, acetyl chloride (8 μL, 0.12 mmol) and 4-(dimethylamino)pyridine (DMAP) (5 mg, 0.03 mmol) were added, the resulting mixture was stirred at room temperature for 15 min. Then the solution was washed with water and the organic layer was dried over Na2SO4, filtered and the solvent removed under reduced pressure to obtain 18 mg (yield 66%) of 25a as a red oil. 1H-NMR (CDCl3): 2.10 (s, 3H), 3.88 (s, 3H), 4.20 (s, 2H), 7.00-7.02 (m, 2H), 7.22-7.33 (m, 8H), 7.61-7.64 (m, 4H), 7.68 (s, 1H). MS (ESI): m/z 482 (M+H+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08546147B2uspto-grants-2013_10