반응 #326177

ord-84b9bfb18bbe48c0987fa54d56495d84

반응 조건

온도
27.5°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas charged at 25-30° C
  2. 2
    기타Solid obtained
  3. 3
    여과was filtered
  4. 4
    세척washed with SPDS
  5. 5
    기타dried under vacuum
  6. 6
    workup.STIRRINGstirred for 10 minutes

실험 절차

5 g of 4-chloro-6,7-bis(2-methoxyethoxy) quinazoline was suspended in 150 ml denatured spirit (SPDS) and 4.6 g of 3-aminophenyl acetylene was charged at 25-30° C. Further 1.0 ml of methane sulphonic acid was added. The reaction mass was stirred at 25-30° C. for 3 hours. Solid obtained was filtered, washed with SPDS and dried under vacuum. This solid was suspended in water, basified with ammonia and stirred for 10 minutes. The resulting erlotinib base was isolated, washed with water and dried under vacuum. The base was suspended in water and acidified to pH 1.0-2.0 using hydrochloric acid. The reaction mixture was stirred for 2 hours, filtered, washed with water and dried at 40-45° C. to obtain 5.8 g of erlotinib hydrochloride.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08642758B2uspto-grants-2014_02