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HRID 448038作成日:2026年10月26日

Norborn-2-ylacetic acid → (3Z)-1-[bicyclo[2.2.1]hept-2-yl]-3-(3-butyl-5-methyl-1,3,4-thiadiazol-2(3H)-ylidene)acetone

https://huagongshe.com/reaction/448038

反応式

関与物質

役割名称HCID仕込み量
反応物Norborn-2-ylacetic acidHCID 79139—
反応物DiisopropylethylamineHCID 81531—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物3-Butyl-2,5-dimethyl-1,3,4-thiadiazol-3-ium iodideHCID 69187917—
生成物(3Z)-1-[bicyclo[2.2.1]hept-2-yl]-3-(3-butyl-5-methyl-1,3,4-thiadiazol-2(3H)-ylidene)acetoneHCID 69187940—

反応手順

In a 20 mL vial 2-(bicyclo[2.2.1]heptan-2-yl)acetic acid (0.9 mL of 0.2 M in DMA, 1.10 equiv) was added followed by the addition of HATU (77 mg in 0.7 mL of DMA, 0.2 mmol, 1.20 equiv.), DIEA (53 mg in 0.7 mL of DMA, 0.4 mmol, 2.40 equiv.), and finally 3-butyl-2,5-dimethyl-1,3,4-thiadiazol-3-ium iodide (50 mg in 0.7 mL of DMA, 0.17 mmol, 1 equiv.). The mixture was shaken overnight at room temperature and then concentrated in vacuo. The resulting residue was taken up in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.90 (t, 3H) 0.98-1.18 (m, 4 H) 1.23-1.49 (m, 6 H) 1.62-1.73 (m, 2 H) 1.80-1.88 (m, 1 H) 1.89-1.95 (m, 1 H) 2.11-2.19 (m, 2 H) 2.23-2.31 (m, 1 H) 2.38-2.43 (m, 3 H) 4.02 (t, 2 H) 5.86-5.92 (m, 1 H); MS (ESI) m/z 307 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481574B2
出典データセットuspto-grants-2013_07
ORD IDord-f15e509d56184c7ab9958b1ac95539bd
出典メモuspto-grants-2013_07