반응 #48842

ord-a834994161f4422b977882c441c78710

반응 방정식

Cc1cnc(NC(=O)c2cc(OCc3ccccc3)cc(O[C@@H](C)CO[Si](C)(C)C(C)(C)C)c2)s1
3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide
CCN(CC)CC
Triethylamine
CC[SiH](CC)CC
triethylsilane
Cc1cnc(NC(=O)c2cc(O)cc(O[C@@H](C)CO)c2)s1
desired compound
수율 21.4%
Cc1cnc(NC(=O)c2cc(O)cc(O[C@@H](C)CO)c2)s1
3-Hydroxy-5-[(1S)-2-hydroxy-1-methylethoxy]-N-(5-methyl-1,3-thiazol-2-yl)benzamide
수율 21.4%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGstirred for a further 48 hours
  2. 2
    여과The reaction was filtered through celite
  3. 3
    농축the filtrate concentrated in vacuo
  4. 4
    기타to give a residue which
  5. 5
    기타was chromatographed on silica
  6. 6
    세척eluting with a gradient of 50-100% ethyl acetate in isohexane

실험 절차

Triethylamine (0.11 mL, 0.79 mmol) and triethylsilane (4.88 mL, 27.3 mmol) were added to palladium (11) acetate (56 mg, 9 mol %) in DCM (14 mL) under an atmosphere of argon. The reaction was stirred for 15 mins then 3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide (1.4 g, 2.73 mmol) in DCM (14 mL) added dropwise and stirred for a further 48 hours. The reaction was filtered through celite and the filtrate concentrated in vacuo to give a residue which was chromatographed on silica, eluting with a gradient of 50-100% ethyl acetate in isohexane, to give the desired compound (0.18 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745475B2uspto-grants-2010_06