Acetic Acid → [2-(4-Cyclopropylpiperazin-1-yl)benzooxazol-5-ylmethyl]dimethylamine
반응식
[CH:1]1([N:4]2[CH2:9][CH2:8][N:7]([C:10]3[O:11][C:12]4[CH:18]=[CH:17][C:16]([CH:19]=O)=[CH:15][C:13]=4[N:14]=3)[CH2:6][CH2:5]2)[CH2:3][CH2:2]1.Cl.[CH3:22][NH:23][CH3:24].C(O)(=O)C.[BH3-]C#N.[Na+]>CO.C1COCC1>[CH:1]1([N:4]2[CH2:9][CH2:8][N:7]([C:10]3[O:11][C:12]4[CH:18]=[CH:17][C:16]([CH2:19][N:23]([CH3:24])[CH3:22])=[CH:15][C:13]=4[N:14]=3)[CH2:6][CH2:5]2)[CH2:3][CH2:2]1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 2-(4-cyclopropylpiperazin-1-yl)benzooxazole-5-carboxaldehyde (350 mg, 1.29 mmol) and dimethylamine hydrochloride (210 mg, 2.58 mmol) in CH3OH/THF (32 mL, 1:3) was added acetic acid (124 mg, 2.06 mmol), followed by NaCNBH3 (120 mg, 2.06 mmol). The mixture was heated at reflux for 12 h. The volatiles were removed under reduced pressure and the residue was diluted with water (5 mL). The mixture was extracted with CH2Cl2 (3×10 mL) and the combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified by the preparative HPLC to give 233 mg (60%) of [2-(4-cyclopropylpiperazin-1-yl)benzooxazol-5-ylmethyl]dimethylamine as a trifluoroacetate salt.
후처리
- temperatureThe mixture was heated
- temperatureat reflux for 12 h
- customThe volatiles were removed under reduced pressure
- additionthe residue was diluted with water (5 mL)
- extractionThe mixture was extracted with CH2Cl2 (3×10 mL)
- dry with materialthe combined organic extracts were dried (Na2SO4)
- concentrationconcentrated
- customThe residue was purified by the preparative HPLC
출처 및 근거
- ORD 기록
- ord-02dd4833bd094d159a92625507b3aee0
- 출처 데이터셋
- uspto-grants-2013_03
- 특허 번호
- US08394842B2
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