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Potassium Carbonate → 3-chloro-2-methoxy-5-methyl-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine

HRID 597910
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HRID 597910 반응식
COC1C=CC2C(C)CN(C(=O)C(F)(F)F)CCC=2N=1.P(Cl)(Cl)(Cl)(Cl)Cl.O=P(Cl)(Cl)Cl.C([O-])(O)=O.[Na+].[Cl:37][C:38]1[C:55]([O:56][CH3:57])=[N:54][C:41]2[CH2:42][CH2:43][N:44](C(=O)C(F)(F)F)[CH2:45][CH:46]([CH3:47])[C:40]=2[CH:39]=1.C([O-])([O-])=O.[K+].[K+]>CO.C(Cl)Cl>[Cl:37][C:38]1[C:55]([O:56][CH3:57])=[N:54][C:41]2[CH2:42][CH2:43][NH:44][CH2:45][CH:46]([CH3:47])[C:40]=2[CH:39]=1
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참가 물질

9

반응물 6

HCID 11430Potassium CarbonateHCID 24813Phosphorus oxychlorideHCID 24819Phosphorus pentachlorideHCID 516892Sodium BicarbonateHCID 236541072-methoxy-5-methyl-7-(trifluoroacetyl)-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepineHCID 236541103-chloro-2-methoxy-5-methyl-7-(trifluoroacetyl)-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine

생성물 1

HCID 236538053-chloro-2-methoxy-5-methyl-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매

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온도
125 °C

실험 절차

A mixture of 2-methoxy-5-methyl-7-(trifluoroacetyl)-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine (100 mg, 347 μmol), PCl5 (722 mg, 3.47 mmol) and POCl3 (10 ml) was heated at 125° C. in a sealed tube for 16 h. The reaction mixture was parted between DCM and sat. aq. NaHCO3. The organic phase was washed with brine, dried over Na2SO4 and concentrated in vacuo. Chromatographic purification rendered 23.5 mg (21%) of 3-chloro-2-methoxy-5-methyl-7-(trifluoroacetyl)-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine. A mixture of 3-chloro-2-methoxy-5-methyl-7-(trifluoroacetyl)-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine (23.5 mg, 72.8 μmol) and K2CO3 (30 mg) in MeOH (7 ml) was heated at reflux for 2 h. The reaction mixture was concentrated in vacuo and chromatographic purification of the resulting residue rendered 11.2 mg (68%) of 3-chloro-2-methoxy-5-methyl-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine. 1H-NMR (CDCl3) δ 7.48 (s, 1H), 3.99 (s, 3H), 3.55-3.30 (m, 4H), 3.25 (m, 1H), 3.07 (m, 1H), 2.85 (dd, 1H), 1.43 (d, 3H) ppm.

후처리

  1. washThe organic phase was washed with brine
  2. dry with materialdried over Na2SO4
  3. concentrationconcentrated in vacuo
  4. customChromatographic purification
  5. temperaturewas heated
  6. temperatureat reflux for 2 h
  7. concentrationThe reaction mixture was concentrated in vacuo and chromatographic purification of the resulting residue

출처 및 근거

ORD 기록
ord-6370fb5488be44dfaa34697a5100097f
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07897595B2

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