반응 #6975

ord-dcdd4dc25d754501bcc4494e4162c584

반응 방정식

O=Cc1cnc(Nc2ccccn2)s1
2-(pyridin-2-ylamino)-thiazole-5-carbaldehyde
O=Cc1cnc(Nc2ccccn2)s1
compound 1A
O=Cc1cnc(Nc2ccccn2)s1
2-(pyridin-2-ylamino)-thiazole-5-carbaldehyde
Nc1cc(C(=O)O)ccc1F
3-amino-4-fluorobenzoic acid
CC[SiH](CC)CC
triethylsilane
O=C(O)c1ccc(F)c(NCc2cnc(Nc3ccccn3)s2)c1
4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid
수율 91.3%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwere added
  2. 2
    기타The above reaction mixture
  3. 3
    농축concentrated in vacuo
  4. 4
    기타the resulting slurry was triturated with methanol

실험 절차

To a suspension of 2-(pyridin-2-ylamino)-thiazole-5-carbaldehyde (1.0 g, 4.90 mmol, compound 1A) in methylene chloride (20 mL) at RT 3-amino-4-fluorobenzoic acid (0.95 g, 4.90 mmol) TFA (5 mL) and triethylsilane (1.71 mg, 14.7 mmol) were added. The above reaction mixture was stirred at RT for 4 h, then concentrated in vacuo and the resulting slurry was triturated with methanol to afford 4-fluoro-3-{[2-(pyridin-2-ylamino)-thiazol-5-ylmethyl]-amino}-benzoic acid as light yellow solid (1.54 g, 91%) (M+H)+=345.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07084160B2uspto-grants-2006_08