N-Cyclopropylmethyl-N-(2-ethyl-7-iodopyrazolo[1,5-a]pyridin-3-yl)-N-tetrahydro-2H-4-pyranylmethylamine hydrochloride → N-Cyclopropylmethyl-2-ethyl-7-iodo-N-(tetrahydro-2H-pyran-4-ylmethyl)pyrazolo[1,5-a]pyridine-3-amine
반응식
Cl.[CH:2]1([CH2:5][N:6]([CH2:19][CH:20]2[CH2:25][CH2:24][O:23][CH2:22][CH2:21]2)[C:7]2[C:8]([CH2:17][CH3:18])=[N:9][N:10]3[C:15]([I:16])=[CH:14][CH:13]=[CH:12][C:11]=23)[CH2:4][CH2:3]1.O.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C>[CH:2]1([CH2:5][N:6]([CH2:19][CH:20]2[CH2:21][CH2:22][O:23][CH2:24][CH2:25]2)[C:7]2[C:8]([CH2:17][CH3:18])=[N:9][N:10]3[C:15]([I:16])=[CH:14][CH:13]=[CH:12][C:11]=23)[CH2:4][CH2:3]1참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
To N-cyclopropylmethyl-2-ethyl-7-iodo-N-(tetrahydro-2H-pyran-4-ylmethyl)pyrazolo[1,5-a]pyridine-3-amine hydrochloride (16 g) was added saturated sodium bicarbonate water (200 mL) to give neutrality. Then, ethyl acetate (100 mL) was added to this, and an organic layer was separated. From the organic layer, the solvent was distilled off under reduced pressure. Into the resulting residue was dropped acetonitrile (30 mL) and water (120 mL), the mixture was stirred overnight, and the resulting precipitate was filtrated. The precipitate was dried under reduced pressure, and 13 g of a title compound was obtained as white crystal.
후처리
- customto give neutrality
- customwas separated
- distillationFrom the organic layer, the solvent was distilled off under reduced pressure
- additionInto the resulting residue was dropped acetonitrile (30 mL) and water (120 mL)
- filtrationthe resulting precipitate was filtrated
- customThe precipitate was dried under reduced pressure
출처 및 근거
- ORD 기록
- ord-b19a3fbd708d468ea5ce281b5fdcec74
- 출처 데이터셋
- uspto-grants-2010_12
- 특허 번호
- US07858809B2
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