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Formaldehyde → (3S,4S)-4-(4-bromo-2-nitrophenylamino)-1-methylpyrrolidin-3-ol

HRID 1670622
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HRID 1670622 반응식
Cl.[Br:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C@H:10]2[CH2:14][NH:13][CH2:12][C@@H:11]2[OH:15])=[C:5]([N+:16]([O-:18])=[O:17])[CH:4]=1.[C:19](O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C=O.C(=O)(O)[O-].[Na+]>C(#N)C>[Br:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C@H:10]2[CH2:14][N:13]([CH3:19])[CH2:12][C@@H:11]2[OH:15])=[C:5]([N+:16]([O-:18])=[O:17])[CH:4]=1
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참가 물질

6

반응물 4

HCID 712FormaldehydeHCID 516892Sodium BicarbonateHCID 5049666Sodium triacetoxyborohydrideHCID 67336101(3S,4S)-4-(4-Bromo-2-nitro-phenylamino)-pyrrolidin-3-ol hydrochloride

생성물 1

HCID 57748725(3S,4S)-4-(4-bromo-2-nitrophenylamino)-1-methylpyrrolidin-3-ol수율 103.4%

시약·촉매·용매 1

HCID 6342
Acetonitrile
용매

실험 절차

To (3S,4S)-4-(4-Bromo-2-nitro-phenylamino)-pyrrolidin-3-ol hydrochloride (0.104 mol, 35.0 g) in acetonitrile add sodium triacetoxyborohydride (0.37 mol, 78.0 g) at 0° C. To this mixture, add slowly 37% aqueous formaldehyde (30 mL) over 10 min and stir at room temperature for 10 h. Add saturated aqueous sodium bicarbonate and stir for one hour. Extract with ethyl acetate, and wash with water and brine. Dry over anhydrous sodium sulfate, filter, and evaporate the solvent to obtain the title compound as a yellow solid (34.0 g, 98%). APCI MS m/z 302 [M+H]+; [α]23D +58.6° (c, 0.50, MeOH).

후처리

  1. extractionExtract with ethyl acetate
  2. washwash with water and brine
  3. dry with materialDry over anhydrous sodium sulfate
  4. filtrationfilter
  5. customevaporate the solvent

출처 및 근거

ORD 기록
ord-948a80ccae044e8cbfa926ea86b202b3
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994164B2

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