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

HRID 2267198노트

반응식

HRID 2267198 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]1

참가 물질

4

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

  1. customto give neutrality
  2. customwas separated
  3. distillationFrom the organic layer, the solvent was distilled off under reduced pressure
  4. additionInto the resulting residue was dropped acetonitrile (30 mL) and water (120 mL)
  5. filtrationthe resulting precipitate was filtrated
  6. 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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