반응 #160661

ord-12c24e16ac7245f5892b4517493a0d94

반응 방정식

Cc1cc(C)nc(N)c1
4,6-dimethyl-2-aminopyridine
CC(=O)CCC(C)=O
acetonylacetone
Cc1cc(C)nc(-n2c(C)ccc2C)c1
8
수율 91.0%
Cc1cc(C)nc(-n2c(C)ccc2C)c1
2-(2,5-Dimethyl-1H-pyrrol-1-yl)-4,6-dimethylpyridine
수율 91.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction mixture was heated in a Dean-Stark apparatus
  2. 2
    온도under reflux for 6 h
  3. 3
    농축the mixture was concentrated with a rotary evaporator
  4. 4
    기타the resulting brown oil was purified by flash column chromatography (EtOAc/hexanes, 1:19-1:9)

실험 절차

To a solution of 4,6-dimethyl-2-aminopyridine (7, 12.2 g, 100 mmol) in toluene (100 mL) was added acetonylacetone (12.3 mL, 105 mmol) and p-TsOH (190 mg, 1.0 mmol). The reaction mixture was heated in a Dean-Stark apparatus under reflux for 6 h. After cooling to room temperature, the mixture was concentrated with a rotary evaporator, and the resulting brown oil was purified by flash column chromatography (EtOAc/hexanes, 1:19-1:9) to give 8 (18.2 g, 91 mmol, 91%) as a pale yellow solid: 1H NMR (500 MHz, CDCl3) δ 2.13 (s, 6H), 2.40 (s, 3H), 2.56 (s, 3H), 5.88 (s, 2H), 6.85 (s, 1H), 7.00 (s, 1H); 13C NMR (125 MHz, CDCl3) δ 13.4, 21.2, 24.4, 106.8, 119.9, 123.1, 128.6, 149.6, 151.7, 158.4; LCQ-MS (M+H+) calcd for C13H17N2 201. found 201; LC-TOF-MS (M+H+) calcd for C13H17N2 201.13917. found 201.13881.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08829187B1uspto-grants-2014_09