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Trimethylsilyldiazomethane → Methyl 2-(5-amino-4-methyl-2-pyridinyl)acetate

HRID 1502122
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HRID 1502122 반응식
[CH3:1][C:2]1[C:7]([NH:8]C(=O)C(C)(C)C)=[CH:6][N:5]=[C:4]([CH2:15][C:16]([O:18][C:19](C)(C)C)=[O:17])[CH:3]=1.[Si](C=[N+]=[N-])(C)(C)C>Cl>[NH2:8][C:7]1[C:2]([CH3:1])=[CH:3][C:4]([CH2:15][C:16]([O:18][CH3:19])=[O:17])=[N:5][CH:6]=1
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참가 물질

4

반응물 2

HCID 167693TrimethylsilyldiazomethaneHCID 89619062Tert-butyl 2-(4-methyl-5-pivalamidopyridin-2-yl)acetate

생성물 1

HCID 89619043Methyl 2-(5-amino-4-methyl-2-pyridinyl)acetate

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

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온도
0 °C

실험 절차

Tert-butyl 2-(4-methyl-5-pivalamidopyridin-2-yl)acetate (0.200 g, 0.653 mmol) was refluxed in hydrochloric acid 6N (10 ml) overnight. The reaction was concentrated then re-dissolved in MeOH (10 ml) and cooled to 0° C. then added TMS-diazomethane (0.653 ml, 1.305 mmol). When no SM was observed by TLC, the reaction was quenched with glacial acetic acid and concentrated. The residue was taken up with ethyl acetate and washed with NaHCO3. The organic layer was dried over NaSO4, filtered and evaporated to dryness. The residue was purified by chromatography using 40 g ISCO Redisep column and 5% MeOH/DCM solvent system to yield title compound.

후처리

  1. concentrationThe reaction was concentrated
  2. dissolutionthen re-dissolved in MeOH (10 ml)
  3. customthe reaction was quenched with glacial acetic acid
  4. concentrationconcentrated
  5. washwashed with NaHCO3
  6. dry with materialThe organic layer was dried over NaSO4
  7. filtrationfiltered
  8. customevaporated to dryness
  9. customThe residue was purified by chromatography

출처 및 근거

ORD 기록
ord-9e8beb806e2f471f9342c5224b1224ab
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09206199B2

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