Iodine → HCID 939755, 화합물

HRID 343878노트

반응식

HRID 343878 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:10]([Cl:11])=[C:9]([C:12](OC)=[O:13])[S:8][C:7]=2[CH:16]=1.CO.[NH2:19][NH2:20].II>C(OCC)(=O)C.CCCCCC>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:10]([Cl:11])=[C:9]([C:12]([NH:19][NH2:20])=[O:13])[S:8][C:7]=2[CH:16]=1

참가 물질

7

실험 절차

A 100 ml, round bottomed flask, reflux condenser, gas inlet and Teflon stirrer were oven dried for 12 hours at 160° C. The apparatus was rapidly assembled, flushed with dry nitrogen gas, and cooled to room temperature. The reaction flask was charged with methyl 6-methoxy-3-chlorobenzo[b]thiophene-2-carboxylate (1.50 g, 5.85 mmole), anhydrous methanol (Aldrich, 50 ml), and anhydrous hydrazine (Aldrich, 2.5 equivalents, 0.47 g, 0.45 ml, 14.61 mmole). The stirred reaction mixture was brought to reflux and the progress of the reaction monitored by TLC (Silica, 1:1 hexane:ethyl acetate, iodine and UV visualization). After 72 hours, the completed reaction was cooled to room temperature, and further cooled to 5° C. for 1 hour. The resulting solid was filtered, washed with cold methanol (2×10 ml), and dried in vacuo. This resulted in 0.856 g of the desired material, as a white amorphous powder which was used directly.

후처리

  1. temperatureA 100 ml, round bottomed flask, reflux condenser, gas inlet and Teflon stirrer
  2. customdried for 12 hours at 160° C
  3. customflushed with dry nitrogen gas
  4. customThe stirred reaction mixture
  5. temperatureto reflux
  6. customthe completed reaction
  7. temperaturewas cooled to room temperature
  8. temperaturefurther cooled to 5° C. for 1 hour
  9. filtrationThe resulting solid was filtered
  10. washwashed with cold methanol (2×10 ml)
  11. customdried in vacuo

출처 및 근거

ORD 기록
ord-c1df27f3edd645c9beaae5186e5fccd7
출처 데이터셋
uspto-grants-1999_01
특허 번호
US05863936

반응 노트

불러오는 중…