반응 #8935

ord-5233044755d24604977768d373a36afd

반응 방정식

CCOC(C)=O
ethyl acetate
Cc1ccccc1C(=O)Cl
ortho-toluoyl chloride
CCN(CC)CC
triethylamine
NC(=O)c1ccccc1
benzamide

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with 5% citric acid, saturated sodium bicarbonate, brine
  2. 2
    기타dried
  3. 3
    여과filtered
  4. 4
    농축concentrated
  5. 5
    기타to afford 420 mg of crude material
  6. 6
    기타This was chromatographed on 40 g of silica gel using 50% ethyl acetate/hexane

실험 절차

To a solution of 391 mg (1 mmol) of 2R-hydroxy-3-[(2-methylpropyl)(4-aminophenyl)sulfonyl]amino-1S-(phenylmethyl)propylamine in 3 mL of anhydrous methylene chloride, was added 0.42 mL (3 mmol) of triethylamine, then at room temperature, 0.12 mL (0.9 mmol) of ortho-toluoyl chloride was added. After 15 hours at room temp ethyl acetate was added, washed with 5% citric acid, saturated sodium bicarbonate, brine, dried, filtered and concentrated to afford 420 mg of crude material. This was chromatographed on 40 g of silica gel using 50% ethyl acetate/hexane to afford 368 mg of pure benzamide, N-[2R-hydroxy-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl) amino]-1S-(phenylmethyl)propyl]-2-methyl, m/e=516 (M+Li).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07091219B2uspto-grants-2006_08