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Tert-butyl 4-(2-methyl-4-nitro-pyrazol-3-yl)-1,4-diazepane-1-carboxylate → 1-(2-Methyl-4-nitro-pyrazol-3-yl)-1,4-diazepane

HRID 1915923
ノート
印刷プレビュー

反応式

HRID 1915923 の反応式
[CH3:1][N:2]1[C:6]([N:7]2[CH2:13][CH2:12][CH2:11][N:10](C(OC(C)(C)C)=O)[CH2:9][CH2:8]2)=[C:5]([N+:21]([O-:23])=[O:22])[CH:4]=[N:3]1>C(Cl)Cl.C(O)(C(F)(F)F)=O>[CH3:1][N:2]1[C:6]([N:7]2[CH2:13][CH2:12][CH2:11][NH:10][CH2:9][CH2:8]2)=[C:5]([N+:21]([O-:23])=[O:22])[CH:4]=[N:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 86680122Tert-butyl 4-(2-methyl-4-nitro-pyrazol-3-yl)-1,4-diazepane-1-carboxylate

生成物 1

HCID 866801231-(2-Methyl-4-nitro-pyrazol-3-yl)-1,4-diazepane収率 64%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 6422Trifluoroacetic acid溶媒

実験手順

A solution of tert-butyl 4-(2-methyl-4-nitro-pyrazol-3-yl)-1,4-diazepane-1-carboxylate (200 mg, 0.61 mmol) in DCM (4 mL) and TFA (4 mL) was stirred at room temperature for 1 h. The solvent was removed under reduced pressure, basified with saturated NaHCO3, and extracted with ethyl acetate (3×). The combined organic layers were dried over MgSO4 and the solvent removed under reduced pressure and the residue purified via silica gel column chromatography (0-10% methanol/DCM) to gave 1-(2-methyl-4-nitro-pyrazol-3-yl)-1,4-diazepane (88 mg, 64%). This was dissolved in acetonitrile (3 mL). tert-Butyl 3-iodoazetidine-1-carboxylate (221 mg, 0.78 mmol) and DIPEA (5 eq) were added and the mixture was heated at 75° C. for 7 days, with additional iodide and DIPEA added on days 2 and 3. The reaction mixture was cooled to room temperature, water (20 ml) was added and the mixture was extracted with DCM (50 mL). The organic layer was washed with water (20 mL), separated, dried over MgSO4 and the solvent removed under reduced pressure. Purification via silica gel column chromatography (0-10% methanol/DCM) to gave tert-butyl 3-[4-(2-methyl-4-nitro-pyrazol-3-yl)-1,4-diazepan-1-yl]azetidine-1-carboxylate (144 mg, 97%).

後処理

  1. customThe solvent was removed under reduced pressure
  2. extractionextracted with ethyl acetate (3×)
  3. dry with materialThe combined organic layers were dried over MgSO4
  4. customthe solvent removed under reduced pressure
  5. customthe residue purified via silica gel column chromatography (0-10% methanol/DCM)

出典と根拠

ORDレコード
ord-04e0069061af4ebc9b8d75c213ac5f95
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08614206B2

反応ノート

読み込み中…

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