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Hydrochloric Acid → HCID 66894903, 화합물

HRID 1257531
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HRID 1257531 반응식
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:9]=[C:10]([CH:18]=[C:19]([C:21]3[CH2:25][C@@H:24]([C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=4)[O:23][N:22]=3)[CH:20]=2)[C:11]([O:13]C(C)(C)C)=[O:12])=[N:6][CH:7]=1.Cl>ClCCl>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:9]=[C:10]([CH:18]=[C:19]([C:21]3[CH2:25][C@@H:24]([C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=4)[O:23][N:22]=3)[CH:20]=2)[C:11]([OH:13])=[O:12])=[N:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 66895837tert-Butyl 3-(5-methylpyridin-2-yl)-5-[(5S)-5-pyridin-2-yl-4,5-dihydroisoxazol-3-yl]benzoate

생성물 1

HCID 66894903HCID 66894903, 화합물수율 123%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of tert-butyl 3-(5-methylpyridin-2-yl)-5-[(5S)-5-pyridin-2-yl-4,5-dihydroisoxazol-3-yl]benzoate (18.6 g, 44.8 mmol) in dichloromethane (100 mL) was added hydrogen chloride (4.0 M in dioxane; 56.0 mL, 224 mmol). The reaction mixture was stirred at ambient temperature. After 18 h, the mixture was concentrated. Dichloromethane was added the suspension was filtered. The solid cake was washed with dihchloromethane and dried under reduced pressure gave the hydrochloride salt of the title compound (19.8 g). MS 359.8 (M+1).

후처리

  1. concentrationthe mixture was concentrated
  2. additionDichloromethane was added the suspension
  3. filtrationwas filtered
  4. washThe solid cake was washed with dihchloromethane
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-66111dace820409c820ccf33beb8b5bf
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08461185B2

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