Methanol → HCID 178525539, 화합물

HRID 2378705노트

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HRID 2378705 반응식
[Cl:1][C:2]1[C:10]2[C:9]3[CH2:11][N:12]([CH2:22][CH2:23][N:24]4[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]4)[C:13](=[O:21])[C@H:14]([CH2:16][C:17]([O:19]C)=[O:18])[CH2:15][C:8]=3[CH:7]=[C:6]([Cl:30])[C:5]=2[NH:4][N:3]=1.O1CCCC1.CO.O.O.[OH-].[Li+]>>[Cl:1][C:2]1[C:10]2[C:9]3[CH2:11][N:12]([CH2:22][CH2:23][N:24]4[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]4)[C:13](=[O:21])[C@H:14]([CH2:16][C:17]([OH:19])=[O:18])[CH2:15][C:8]=3[CH:7]=[C:6]([Cl:30])[C:5]=2[NH:4][N:3]=1

참가 물질

6

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온도
50 °C

실험 절차

(S)-Methyl 2-(1,4-dichloro-8-oxo-9-(2-(piperidin-1-yl)ethyl)-3,6,7,8,9,10-hexahydroazepino[3,4-e]indazol-7-yl)acetate (260 mg, 0.573 mmol) was dissolved in a mixture of tetrahydrofuran (5.0 mL, 61.6 mmol) and methanol (5.0 mL, 123 mmol). Water (5.0 mL, 278 mmol) was added to the mixture followed by lithium hydroxide hydrate (65 mg, 1.549 mmol). Mixture was warmed to 50° C. and held with stirring for 4.5 hours. Mixture was cooled to room temperature. Organic solvents were removed from the mixture by roto-vap. Residue was neutralized with 1.6 mL 1N hydrochloric acid and treated with ethyl acetate. Mixture sat at room temperature for 20 minutes allowing solids to form. Solids were filtered off and washed with water. Solids were dried in vacuo. Title compound was obtained as white solid in 50% yield. MS (M−H)−=437.1, 439.2.

후처리

  1. temperatureMixture was cooled to room temperature
  2. customOrganic solvents were removed from the mixture by roto-vap
  3. additiontreated with ethyl acetate
  4. waitMixture sat at room temperature for 20 minutes
  5. customto form
  6. filtrationSolids were filtered off
  7. washwashed with water
  8. customSolids were dried in vacuo

출처 및 근거

ORD 기록
ord-36067788178b492c828be8dadc4d4885
출처 데이터셋
uspto-grants-2008_12
특허 번호
US07470679B2

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