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Hydroxyamine hydrochloride → HCID 85044904, 화합물

HRID 1986050
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HRID 1986050 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:10][C:11]3[C:16]([C:17](=S)[CH:18]=2)=[CH:15][CH:14]=[CH:13][C:12]=3[CH3:20])=[CH:5][CH:4]=1.Cl.[NH2:22][OH:23]>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:10][C:11]3[C:16]([C:17](=[N:22][OH:23])[CH:18]=2)=[CH:15][CH:14]=[CH:13][C:12]=3[CH3:20])=[CH:5][CH:4]=1
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참가 물질

4

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 86002050HCID 86002050, 화합물

생성물 1

HCID 85044904HCID 85044904, 화합물수율 85.7%

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
110 °C

실험 절차

To a solution of 2-(4-Methoxy-phenyl)-8-methyl-chromene-4-thione (160.0 mg, 0.57 mmol) in 3.5 mL of pyridine was added 118.4 mg (1.70 mmol) of hydroxylamine hydrochloride. The solution was stirred at 110° C. for 1 h. The solvent was removed under vacuum and the residue was treated with ice. The resulting slurry was filtered. The filter cake was washed with H2O and then dried overnight under vacuum to afford 137.0 mg (85.7% yield) of desired compound I-23 as a yellow solid. 1H NMR (500 MHz, DMSO-d6) δ 10.86 (s, 1H), 7.89 (d, 2H), 7.71 (d, 1H), 7.35 (d, 1H), 7.15 (t, 1H), 7.09 (d, 2H), 7.00 (s, 1H), 3.84 (s, 3H), 2.44 (s, 3H) ppm. LC/MS: 282.1 (M+H), 280.0 (M−H), HPLC/Method A (Rt 6.268 min, 95.4% purity).

후처리

  1. customThe solvent was removed under vacuum
  2. additionthe residue was treated with ice
  3. filtrationThe resulting slurry was filtered
  4. washThe filter cake was washed with H2O
  5. customdried overnight under vacuum

출처 및 근거

ORD 기록
ord-f0ded93d715c4c2a9fb7c1efe261b7b8
출처 데이터셋
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07547794B2

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