Carbon Dioxide → N-(2-hydroxybenzyl)-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide

HRID 704242

反応式

HRID 704242 の反応式
B(Br)(Br)Br.C[O:6][C:7]1[CH:38]=[CH:37][CH:36]=[CH:35][C:8]=1[CH2:9][NH:10][C:11]([C:13]1[CH:26]=[CH:25][C:24]2[S:23][C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:16]([CH:27]([CH3:34])[CH2:28][N:29]3[CH2:33][CH2:32][CH2:31][CH2:30]3)[C:15]=2[CH:14]=1)=[O:12].C(=O)([O-])O.[Na+].C(=O)=O>C(Cl)Cl>[OH:6][C:7]1[CH:38]=[CH:37][CH:36]=[CH:35][C:8]=1[CH2:9][NH:10][C:11]([C:13]1[CH:26]=[CH:25][C:24]2[S:23][C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:16]([CH:27]([CH3:34])[CH2:28][N:29]3[CH2:30][CH2:31][CH2:32][CH2:33]3)[C:15]=2[CH:14]=1)=[O:12]

参加物

6

反応物 4

HCID 280Carbon DioxideHCID 25134Boron tribromideHCID 516892Sodium BicarbonateHCID 20074846N-(2-methoxybenzyl)-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide

生成物 1

HCID 20074856N-(2-hydroxybenzyl)-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide収率 41.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
-50 °C

実験手順

A solution of boron tribromide (5.01 g) in methylene chloride (100 cc) is added dropwise and with stirring during 15 minutes to a solution, cooled to -50° C., of N-(2-methoxybenzyl)-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide (4.74 g) in methylene chloride (100 cc). Stirring is maintained at -50° C. for 45 minutes and then at 20° C. for 48 hours. Saturated aqueous sodium hydrogen carbonate solution (120 cc) is then added cautiously. After stirring until the evolution of carbon dioxide has ceased, the organic phase is separated, washed with distilled water (3×100 cc), dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa). The yellow meringue-like residue is purified by chromatography on a column (height: 48 cm; diameter: 2.4 cm) of silica gel (0.06-0.2 mm), eluting with ethyl acetate (2 liters) and collecting 100-cc fractions. Fractions 4 to 15 are combined and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. The yellow meringue-like residue (2.84 g) is purified by chromatography on a column (height: 33 cm; diameter: 2.4 cm) of silica gel (0.06-0.2 mm), eluting successively with a mixture (50:50 by volume) (250 cc) of cyclohexane and ethyl acetate, then with a mixture (25:75 by volume) (500 cc) of cyclohexane and ethyl acetate and then with ethyl acetate (500 cc) and collecting 60-cc fractions. Fractions 7 to 18 are combined and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. to give N-(2-hydroxybenzyl)-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide (1.9 g) in the form of a yellow product of meringue-like consistency.

後処理

  1. stirringStirring
  2. waitat 20° C. for 48 hours
  3. customthe organic phase is separated
  4. washwashed with distilled water (3×100 cc)
  5. dry with materialdried over magnesium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated to dryness under reduced pressure (30 mm Hg; 4 kPa)
  8. customThe yellow meringue-like residue is purified by chromatography on a column (height: 48 cm; diameter: 2.4 cm) of silica gel (0.06-0.2 mm)
  9. washeluting with ethyl acetate (2 liters)
  10. customcollecting 100-cc fractions
  11. concentrationconcentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C
  12. customThe yellow meringue-like residue (2.84 g) is purified by chromatography on a column (height: 33 cm; diameter: 2.4 cm) of silica gel (0.06-0.2 mm)
  13. washeluting successively with a mixture (50:50 by volume) (250 cc) of cyclohexane and ethyl acetate
  14. customwith a mixture (25:75 by volume) (500 cc) of cyclohexane and ethyl acetate and then with ethyl acetate (500 cc) and collecting 60-cc fractions
  15. concentrationconcentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C.

出典と根拠

ORDレコード
ord-fd8777cd2631421a8a5df5c409a74069
出典データセット
uspto-grants-1991_01
特許番号
US04985419

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