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N-methyl-2-pyrrolidone → Methyl 6-cyano-7-fluorochroman-4-carboxylate

HRID 510720
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인쇄 미리보기

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HRID 510720 반응식
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[F:12])[O:8][CH2:7][CH2:6][CH:5]2[C:13]([O:15][CH3:16])=[O:14].[CH3:17][N:18]1CCCC1=O>>[C:17]([C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[F:12])[O:8][CH2:7][CH2:6][CH:5]2[C:13]([O:15][CH3:16])=[O:14])#[N:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 13387N-methyl-2-pyrrolidoneHCID 46929189Methyl 6-bromo-7-fluoro-chromane-4-carboxylate

생성물 1

HCID 67080208Methyl 6-cyano-7-fluorochroman-4-carboxylate수율 77%

반응 조건

온도
160 °C

실험 절차

Methyl 6-bromo-7-fluoro-3,4-dihydro-2H-chromene-4-carboxylate (415 mg, 1.44 mmol) was diluted with N-methylpyrrolidone (5 mL) followed by the addition of Cu(I)CN (643 mg, 7.18 mmol). The reaction was bubbled with argon for 20 minutes, then heated at 160° C. under a slight argon bubble for 6 hours. The reaction was cooled to ambient temperature and loaded directly onto a Biotage 25 column eluting with 5% ethyl acetate/hexanes to 100% ethyl acetate to yield the title compound (260 mg, 77.0% yield).

후처리

  1. customThe reaction was bubbled with argon for 20 minutes
  2. custombubble for 6 hours
  3. temperatureThe reaction was cooled to ambient temperature
  4. washeluting with 5% ethyl acetate/hexanes to 100% ethyl acetate

출처 및 근거

ORD 기록
ord-09c68d1b76e74b43a723aaa1986c67d4
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096567B2

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