JP2022054217A - 化合物又はその塩、及び放射性増感剤 - Google Patents
化合物又はその塩、及び放射性増感剤 Download PDFInfo
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- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H7/00—Compounds containing non-saccharide radicals linked to saccharide radicals by a carbon-to-carbon bond
- C07H7/02—Acyclic radicals
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Abstract
Description
以下、一般式(1)の例として構造式(11)で表されるナトリウム塩を合成する方法の一例について説明を行う。本実施例では、3-(n-オクタデシルオキシ)-n-プロピル-α-D-キノボピラノシドナトリウム塩(構造式(11)において、Cm:nがオクタデシル基)が、上述した経路A~Jにしたがって合成された。
MS:測定値m/z 331.02[M+Na] 計算値 308.33[M]
δ:7.6-7.2(5H)、6.0-3.5(13H)
MS:測定値m/z 513.03[M+Na] 計算値 488.58[M]
δ:7.6-7.2(15H)、6.0-3.5(17H)
MS:測定値m/z 529.28[M+Na] 計算値 506.68[M]
δ:7.6-7.2(15H)、6.0-3.5(16H)、2.0-1.8(2H)
MS:測定値m/z 781.86[M+Na] 計算値 759.08[M]
δ:7.6-7.3(15H)、5.7-3.3(16H)、2.0-9.8(39H)
MS:測定値m/z 784.69[M+Na] 計算値 761.10[M]
δ:7.6-7.3(15H)、5.1-4.6(17H)、2.0-9.8(39H)
MS:測定値m/z 938.61[M+Na] 計算値 915.28[M]
δ:7.8-7.2(19H)、5.1-3.3(11H)、2.5-0.8(42H)
MS:測定値m/z 841.49[M+Na] 計算値 819.20[M]
δ:7.4-7.2(15H)、5.0-3.1(17H)、2.5-0.8(42H)
MS:測定値m/z 824.43[M-Na] 計算値 847.14[M]
δ:7.4-7.2(15H)、5.0-3.1(17H)、2.5-0.8(39H)
MS:測定値m/z 556.16[M+Na] 計算値 576.33[M]
δ:5.0-2.8(17H)、4.8-2.8(11H)、1.0-0.8(37H)
以下、被験化合物として、構造式(11)の化合物(化合物(A))と、特許文献2に記載される、放射性増感剤として用いられるスルホピラノシルアシルプロパンジオール誘導体(化合物(B))とがそれぞれ用いられ、その結果が試験別に図20及び図21に示されている。
被験化合物と有機合成用リパーゼ(富士フィルム和光純薬製、リパーゼPSアマノSD)とをそれぞれ1.3μg/μLとなるようにPBSで調整した。次いで、その反応溶液を展開溶媒(クロロホルム:メタノール=1:1)を用いてTLCで展開して分析した。展開を行う反応溶液としては、反応進行前、2時間時点、及び4時間時点のサンプルが用いられた。また、被験化合物として化合物(A)を用いた反応溶液については、反応18時間時点でのサンプルについても分析を行った。TLCとしてはTLCアルミシート シリカゲル60 F254(Merck製)を使用した。
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