Phosphorus oxychloride → HCID 71534484, 화합물
반응식
[CH:1]([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([C:13]([NH:15][NH2:16])=[O:14])=[N:5]1)([CH3:3])[CH3:2].Cl.[CH:18]1([N:22]2[CH2:27][CH2:26][CH:25]([CH2:28][C:29](O)=O)[CH2:24][CH2:23]2)[CH2:21][CH2:20][CH2:19]1.P(Cl)(Cl)(Cl)=O>>[CH:18]1([N:22]2[CH2:23][CH2:24][CH:25]([CH2:28][C:29]3[O:14][C:13]([C:6]4[C:7]5[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=5)[N:4]([CH:1]([CH3:3])[CH3:2])[N:5]=4)=[N:15][N:16]=3)[CH2:26][CH2:27]2)[CH2:19][CH2:20][CH2:21]1참가 물질
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- 온도
- 0 °C
실험 절차
To the mixture of 1-isopropyl-1H-indazole-3-carboxylic acid hydrazide (120 mg, 0.55 mmol) and (1-cyclobutyl piperidin-4-yl) acetic acid hydrochloride (147 mg, 0.74 mmol, obtained in preparation 6) cooled at 0° C., was added phosphoryl chloride (1.5 mL). The reaction temperature was gradually raised to 100° C. and stirred was 2 hours. Upon completion of the reaction, it was cooled to 0° C. and triturated with hexanes (3×25 mL). The crude product was cooled to 0° C., basified with aqueous sodium hydroxide solution and extracted with 5% methanol in dichloromethane. The combined organic layer was dried over anhydrous sodium sulphate and the solvent was removed under reduced pressure. The crude product was purified by silica gel column chromatography to obtain 3-[5-(1-cyclobutyl piperidin-4-yl methyl)-[1,3,4]oxadiazol-2-yl]-1-isopropyl-1H-indazole (62 mg)
후처리
- temperatureThe reaction temperature was gradually raised to 100° C.
- customUpon completion of the reaction, it
- temperaturewas cooled to 0° C.
- customtriturated with hexanes (3×25 mL)
- temperatureThe crude product was cooled to 0° C.
- extractionextracted with 5% methanol in dichloromethane
- dry with materialThe combined organic layer was dried over anhydrous sodium sulphate
- customthe solvent was removed under reduced pressure
- customThe crude product was purified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-8a8c841d850245b3a9871b4159ef359a
- 출처 데이터셋
- uspto-grants-2015_07
- 특허 번호
- US09079894B2
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