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Lithium hydroxide, monohydrate → 3-[(Dimethylamino)methyl]-5-fluorobenzoic acid

HRID 1426293
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HRID 1426293 반응식
[CH3:1][N:2]([CH2:4][C:5]1[CH:6]=[C:7]([CH:12]=[C:13]([F:15])[CH:14]=1)[C:8]([O:10]C)=[O:9])[CH3:3].O.[OH-].[Li+]>O1CCCC1.O>[CH3:3][N:2]([CH2:4][C:5]1[CH:6]=[C:7]([CH:12]=[C:13]([F:15])[CH:14]=1)[C:8]([OH:10])=[O:9])[CH3:1]
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참가 물질

5

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 69672877Methyl 3-[(dimethylamino)methyl]-5-fluorobenzoate

생성물 1

HCID 696731623-[(Dimethylamino)methyl]-5-fluorobenzoic acid수율 59%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 3-[(dimethylamino)methyl]-5-fluorobenzoate (0.040 g, 0.19 mmol from Step 3) was dissolved in tetrahydrofuran (3 mL) and lithium hydroxide monohydrate (0.0954 g, 2.27 mmol) dissolved in water (1 mL) was added. The reaction was stirred for 3 hours. The crude reaction mixture was purified by preparative HPLC-MS (C18, eluting with a gradient of H2O/MeCN containing 0.15% NH4OH). The eluent containing the desired mass was evaporated using rotary evaporation to afford product (22 mg, 59%), which was used directly in Step 5. LCMS (M+H)+: 198.1.

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후처리

  1. additionwas added
  2. customThe crude reaction mixture
  3. customwas purified by preparative HPLC-MS (C18
  4. washeluting with a gradient of H2O/MeCN containing 0.15% NH4OH)
  5. additionThe eluent containing the desired mass
  6. customwas evaporated
  7. customevaporation

출처 및 근거

ORD 기록
ord-43a2ea5f4f8e4145802181c1e433c6c2
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08933085B2

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