tert-Butyl (2,6-dichloropyridin-4-yl)carbamate → HCID 77231196, 화합물

HRID 1039064노트

반응식

HRID 1039064 반응식
Cl[C:2]1[CH:7]=[C:6]([NH:8][C:9](=[O:15])[O:10][C:11]([CH3:14])([CH3:13])[CH3:12])[CH:5]=[C:4]([Cl:16])[N:3]=1.[CH3:17][Mg]Br>C1COCC1.CN1C(=O)CCC1>[Cl:16][C:4]1[CH:5]=[C:6]([NH:8][C:9](=[O:15])[O:10][C:11]([CH3:14])([CH3:13])[CH3:12])[CH:7]=[C:2]([CH3:17])[N:3]=1

참가 물질

4

반응물 2

HCID 45076485tert-Butyl (2,6-dichloropyridin-4-yl)carbamateHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 77231196HCID 77231196, 화합물

시약·촉매·용매 1

HCID 22156051tetrahydrofuran N-methylpyrrolidinone용매

실험 절차

tert-butyl (2,6-dichloropyridin-4-yl)carbamate (460 mg, 1.75 mmol) from Step 1 of this example, ferric acetylacetonate (309 mg, 0.87 mmol) was added in THF:NMP (1:1, 17.4 mL), methyl magnesium bromide (3 mL [3M], 8.9 mmol) was added drop-wise and stirred for 15 min. The reaction was quenched with ice-cold ammonia chloride saturated solution (100 mL), extracted with ethyl acetate (100 mL), second wash with brine (50 mL). The organic phase was dried by magnesium sulfate and filtered through silica gel (1 inch deep), concentrated and purified by column chromatography through a 50 gram Biotage SNAP KP-Sil™ silica gel cartridge eluting with 10% ethyl acetate/hexanes to give the title compounds as a white solid.

후처리

  1. customThe reaction was quenched with ice-cold ammonia chloride saturated solution (100 mL)
  2. extractionextracted with ethyl acetate (100 mL)
  3. washsecond wash with brine (50 mL)
  4. dry with materialThe organic phase was dried by magnesium sulfate
  5. filtrationfiltered through silica gel (1 inch deep)
  6. concentrationconcentrated
  7. custompurified by column chromatography through a 50 gram Biotage SNAP KP-Sil™ silica gel cartridge
  8. washeluting with 10% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-94126aea81d14cd6be55466919ab2222
출처 데이터셋
uspto-grants-2013_10
특허 번호
US08552022B2

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