Diisopropylethylamine → N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide

HRID 1963723

반응식

HRID 1963723 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([C:8](Cl)=[O:9])[CH2:4][CH2:3]1.[Cl:11][C:12]1[CH:17]=[CH:16][N:15]=[C:14]([NH2:18])[CH:13]=1.C(N(C(C)C)CC)(C)C>C(Cl)Cl>[Cl:11][C:12]1[CH:17]=[CH:16][N:15]=[C:14]([NH:18][C:8]([CH:5]2[CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]2)=[O:9])[CH:13]=1

참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 4365031-Methylpiperidine-4-carbonyl chlorideHCID 5818662-Amino-4-chloropyridine

생성물 1

HCID 69008397N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

반응 조건

온도
0 °C

실험 절차

A flask was flame dried and placed under a nitrogen atmosphere. 1-methylpiperidine-4-carbonyl chloride (1 eq) in anhydrous methylene chloride was added to the flask and brought to 0° C. To this was added the solution containing 4-chloropyridin-2-amine (1 eq), and diisopropylethylamine (5 eq) in anhydrous methylene chloride, which was stirred for 1 hour at 0° C. Reaction concentrated and partitioned between water and ethyl acetate. The organic layer was separated, washed with brine, dried over sodium sulfate and concentrated to give the crude product. Purification on silica gel, 10% methanol in methylene chloride to yield N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide as a slightly yellow crystal solid. HPLC=2.39 min; MS: MH+=254.

후처리

  1. temperatureA flask was flame
  2. customdried
  3. custombrought to 0° C
  4. additionTo this was added the solution
  5. customReaction
  6. concentrationconcentrated
  7. custompartitioned between water and ethyl acetate
  8. customThe organic layer was separated
  9. washwashed with brine
  10. dry with materialdried over sodium sulfate
  11. concentrationconcentrated
  12. customto give the crude product
  13. customPurification on silica gel, 10% methanol in methylene chloride

출처 및 근거

ORD 기록
ord-d29a842058d24a01b12bd799e6ec409a
출처 데이터셋
uspto-grants-2013_04
특허 번호
US08415382B2

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