Dimethylformamide → HCID 86209319, 화합물

HRID 1815051노트

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HRID 1815051 반응식
[O:1]=[S:2]1(=[O:11])[CH2:7][CH2:6][CH:5]([C:8](O)=[O:9])[CH2:4][CH2:3]1.CN(C=O)C.C(Cl)(=O)C(Cl)=O.[CH2:23]([O:25][C:26]#[CH:27])[CH3:24]>C(Cl)Cl.C1COCC1.C(N(CC)CC)C>[CH2:26]([O:25][C:23]1[C:5]2([CH2:6][CH2:7][S:2](=[O:11])(=[O:1])[CH2:3][CH2:4]2)[C:8](=[O:9])[CH:24]=1)[CH3:27]

참가 물질

8

반응물 4

HCID 6228DimethylformamideHCID 61239Ether, ethyl ethynylHCID 65578Oxalyl chlorideHCID 1491755Tetrahydro-2H-thiopyran-4-carboxylic acid 1,1-dioxide

생성물 1

HCID 86209319HCID 86209319, 화합물수율 67%

시약·촉매·용매 3

HCID 6344Dichloromethane용매HCID 8028Tetrahydrofuran용매HCID 8471Triethylamine용매

실험 절차

A solution of 1,1-dioxo-hexahydro-1λ6-thiopyran-4-carboxylic acid (10.2 g, 57.3 mmol) [prepared according to the procedure of Org. Prep. Proc. Int. 1977, 94] and DMF (0.3 ml) in DCM (120 ml) at rt, was treated dropwise with oxalyl chloride and the resulting slurry stirred for 3d. The crude reaction was then concentrated in vacuo to give an oil which was re-dissolved in THF (100 ml), treated with ethoxyacetylene (10 ml, 50% w/w) and triethylamine (10 ml) and the resulting slurry stirred for 10d at rt. Filtration and concentration of the filtrate in vacuo gave a crude oil which was purified by chromatography (SiO2, 30% EtOAc:hexanes) to give the title compound as a yellow oil (8.9 g, 38.6 mmol, 67%). δH (CDCl3, 300K) 4.88 (1H, s), 4.27 (2H, q, J 7.1 Hz), 3.44-3.37 (2H, m), 3.13-3.05 (2H, m), 2.47-2.40 (2H, m), 2.35-2.29 (2H, m), 1.48 (3H, t, J 7.1 Hz); m/z (ES+, 70V) 230.9 (MH+).

후처리

  1. customThe crude reaction
  2. concentrationwas then concentrated in vacuo
  3. customto give an oil which
  4. filtrationFiltration and concentration of the filtrate in vacuo
  5. customgave a crude oil which
  6. customwas purified by chromatography (SiO2, 30% EtOAc:hexanes)

출처 및 근거

ORD 기록
ord-6bad974257d448669f4ff32d4b9dfd94
출처 데이터셋
uspto-grants-2005_04
특허 번호
US06878718B2

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