Triethylamine → (2,2-Difluoro-9-(3-(2-hydroxyethyl)benzyl)-1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)(2-isopropylthiazol-4-yl)methanone

HRID 471076노트

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HRID 471076 반응식
Br[CH2:2][C:3]1[CH:4]=[C:5]([CH2:9][CH2:10][OH:11])[CH:6]=[CH:7][CH:8]=1.FC(F)(F)C(O)=O.[F:19][C:20]1([F:41])[CH2:25][N:24]([C:26]([C:28]2[N:29]=[C:30]([CH:33]([CH3:35])[CH3:34])[S:31][CH:32]=2)=[O:27])[CH2:23][C:22]2([CH2:40][CH2:39][NH:38][CH2:37][CH2:36]2)[O:21]1.C(N(CC)CC)C>C(#N)C>[F:41][C:20]1([F:19])[CH2:25][N:24]([C:26]([C:28]2[N:29]=[C:30]([CH:33]([CH3:35])[CH3:34])[S:31][CH:32]=2)=[O:27])[CH2:23][C:22]2([CH2:40][CH2:39][N:38]([CH2:2][C:3]3[CH:8]=[CH:7][CH:6]=[C:5]([CH2:9][CH2:10][OH:11])[CH:4]=3)[CH2:37][CH2:36]2)[O:21]1

참가 물질

5

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온도
20 °C

실험 절차

2-(3-(Bromomethyl)phenyl)ethanol (example 6, step a) (0.21 g) was added to a mixture of (2,2-difluoro-1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)(2-isopropylthiazol-4-yl)methanone trifluoroacetate (example 44, step b) (0.40 g) and triethylamine (0.37 mL) in acetonitrile (15 mL). The reaction mixture was stirred at 20° C. for 2 hours. The solvent was evaporated under reduced pressure and the residue partitioned between ethyl acetate and brine, the organic layer was dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography using 2.5% methanol in dichloromethane with 1% triethylamine as solvent. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 0.40 g.

후처리

  1. customThe solvent was evaporated under reduced pressure
  2. customthe residue partitioned between ethyl acetate and brine
  3. dry with materialthe organic layer was dried over sodium sulphate
  4. filtrationfiltered
  5. customthe solvent evaporated under reduced pressure
  6. customThe crude product was purified by flash silica chromatography
  7. customPure fractions were evaporated to dryness

출처 및 근거

ORD 기록
ord-5558209d7198497c8a6bb48d9f147910
출처 데이터셋
uspto-grants-2014_01
특허 번호
US08629271B2

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