反应详情
EQUATION
反应方程式
REACTANTS
反应物
2,2-Dimethylpropanoic acid
C5H10O2
Triethylamine
C6H15N
Potassium hydroxide
HKO
未命名化合物
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
Ethyl 4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylate
C10H13NO2S
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of HATU (104 mg, 0.274 mmol) and trimethylacetic acid (28 mg, 0.274 mmol) in DCM (2 mL) was added triethylamine (104 μL, 0.203 mmol). The reaction solution was stirred at room temperature for 30 min. A solution of ethyl 4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylate (20 mg, 0.101 mmol; prepared as described in J. Med. Chem. 2006, 49(15):4623-4637) in DMF (0.5 mL) was added in one portion. The solution was then stirred at room temperature overnight. The solution was then diluted with DCM and washed with saturated aqueous NaHCO3. The aqueous layer was extracted with DCM twice, the combined organic phases were additionally washed with water, brine, dried over anhydrous MgSO4 and concentrated to afford an oil residue. To the material thus obtained was added methanol (2 mL), hydroxylamine hydrochloride (52.1 mg, 0.75 mmol), and potassium hydroxide (84.2 mg, 1.5 mmol). The reaction mixture was heated at 80° C. for 3 h, cooled to room temperature and the solvent removed in vacuo. The solid residue obtained was dissolved in DMSO (1.4 mL) and purified with Gilson prep-HPLC [282 nm, rt=5.2 (12 min), 15-40% MeCN—H2O] to afforded white solid (16.1 mg, 24%) as a white solid. LCMS: (FA) ES+ 283; 1H NMR (d6,DMSO, 400 MHz) δ 11.13 (s, 1 H), 9.08 (s, 1 H), 7.37 (s, 1 H), 4.56 (s, 2 H), 3.83 (t, J=5.8 Hz, 2 H), 2.83 (t, J=5.4 Hz, 2 H), 1.22 (s, 9 H).
WORKUP
后处理
- stirringThe solution was then stirred at room temperature overnight
- washwashed with saturated aqueous NaHCO3
- extractionThe aqueous layer was extracted with DCM twice
- washthe combined organic phases were additionally washed with water, brine
- dry with materialdried over anhydrous MgSO4
- concentrationconcentrated
- customto afford an oil residue
- customTo the material thus obtained
- temperatureThe reaction mixture was heated at 80° C. for 3 h
- temperaturecooled to room temperature
- customthe solvent removed in vacuo
- customThe solid residue obtained
- custompurified with Gilson prep-HPLC [282 nm, rt=5.2 (12 min), 15-40% MeCN—H2O]