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Dimethyl Sulfide → HCID 178481639、化合物

HRID 918751
ノート
印刷プレビュー

反応式

HRID 918751 の反応式
[F:1][C:2]1[C:3](=[NH:21])[N:4]([CH3:20])[C:5](=[O:19])[N:6](S(C2C=CC(OC)=CC=2)(=O)=O)[CH:7]=1.FC(F)(F)C(O)=O.CSC>>[F:1][C:2]1[C:3](=[NH:21])[N:4]([CH3:20])[C:5](=[O:19])[NH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 1068Dimethyl SulfideHCID 6422Trifluoroacetic acidHCID 584879375-fluoro-4-imino-1-(4-methoxyphenylsulfonyl)-3-methyl-3,4-dihydropyrimidin-2(1H)-one

生成物 1

HCID 178481639HCID 178481639、化合物

実験手順

A 25-mL screw capped vial was charged with 5-fluoro-4-imino-1-(4-methoxyphenylsulfonyl)-3-methyl-3,4-dihydropyrimidin-2(1H)-one (80.4 mg, 0.257 mmol), trifluoroacetic acid (TFA; 16.0 mL, 215 mmol), and dimethylsulfide (94 μL, 1.28 mmol). The resulting solution was allowed to stir at room temperature for 5.5 h and was then concentrated to dryness by rotary evaporation at 30° C. The crude material was then dissolved in a minimal amount of methanol (CH3OH; ˜2 mL) and loaded onto a 5-g normal phase solid load Isco cartridge, rinsing the source vial with CH3OH (3×1 mL). The solid cartridge was then dried under vacuum at room temperature. After drying, the product was purified by chromatography (4 g SiO2 column; 0 to 30% CH3OH in dichloromethane (CH2Cl2) gradient). The material thus obtained was determined to be the 4-methoxysulfonic acid salt of the desired product. The free base was obtained by dissolving the material in CH3OH (4 mL), adding MP-carbonate resin (345 mg, 3.03 mmol/g, 4.0 equiv), and allowing to stir at room temperature. After stirring for 20 h, the solid resin was filtered off and rinsed with CH3OH (3×1 mL). After concentration under high vacuum, 5-fluoro-4-imino-3-methyl-3,4-dihydropyrimidin-2(1H)-one (35.2 mg, 96%) was obtained as a 95% pure white solid: mp 181-184° C.; 1H NMR (400 MHz, DMSO-d6) δ 7.48 (d, J=4.1 Hz, 1H), 3.22 (s, 3H); 13C NMR (101 MHz, DMSO-d6) δ 152.19 (s), 151.86 (d, J=27.3 Hz), 136.73 (d, J=221.0 Hz), 129.45 (d, J=26.0 Hz), 28.91 (s).

後処理

  1. customA 25-mL screw capped vial
  2. concentrationwas then concentrated to dryness by rotary evaporation at 30° C
  3. dissolutionThe crude material was then dissolved in a minimal amount of methanol (CH3OH; ˜2 mL)
  4. washrinsing the source vial with CH3OH (3×1 mL)
  5. customThe solid cartridge was then dried under vacuum at room temperature
  6. customAfter drying
  7. customthe product was purified by chromatography (4 g SiO2 column; 0 to 30% CH3OH in dichloromethane (CH2Cl2) gradient)
  8. customThe material thus obtained

出典と根拠

ORDレコード
ord-c2554069789c4abbbd6ba3e156c0101e
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09271497B2

反応ノート

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