반응 #966780

ord-0bd904c5b2a9405aabba2b4fc8999583

반응 방정식

COC(=O)[C@@H](OC(C)(C)C)c1c(C)cc2nc(-c3ccnc(Cl)n3)sc2c1-c1ccc(Cl)cc1
(S)-methyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-chloropyrimidin-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetate
CCCN1CCNCC1
1-(3-propyl)-piperazine
C1COCCO1
1,4-dioxane
CCC(CC)N1CCN(c2nccc(-c3nc4cc(C)c([C@H](OC(C)(C)C)C(=O)OC)c(-c5ccc(Cl)cc5)c4s3)n2)CC1
(S)-methyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(4-(pentan-3-yl)piperazin-1-yl)pyrimidin-4-yl)benzo[d]thiazol-6-yl)acetate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAIT40° C. for 1 h
  2. 2
    기타Upon completion of the reaction
  3. 3
    여과the reaction mixture was filtered through Celite (ethyl acetate eluent)
  4. 4
    농축concentrated
  5. 5
    기타used without further purification

실험 절차

To (S)-methyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-chloropyrimidin-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetate (40.0 mg, 0.077 mmol) was added 1-(3-propyl)-piperazine (60.5 mg, 0.387 mmol) in 1,4-dioxane (1 mL). The reaction mixture was stirred at room temperature for 20 min, then 40° C. for 1 h. Upon completion of the reaction, the reaction mixture was filtered through Celite (ethyl acetate eluent), concentrated, and used without further purification. LCMS-ESI+ calc'd for C34H43ClN5O3S (M+H+): 636.3; Found: 636.2 (M+H+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08987250B2uspto-grants-2015_03