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Bromine → (z)-Methyl 4-(7-bromo-2-oxo-2,3-dihydro-1h-thieno[2,3-e][1,4]diazepin-5-yl)benzoate

HRID 1946654
ノート
印刷プレビュー

反応式

HRID 1946654 の反応式
[O:1]=[C:2]1[NH:8][C:7]2[S:9][CH:10]=[CH:11][C:6]=2[C:5]([C:12]2[CH:21]=[CH:20][C:15]([C:16]([O:18][CH3:19])=[O:17])=[CH:14][CH:13]=2)=[N:4][CH2:3]1.[Br:22]Br>N1C=CC=CC=1>[Br:22][C:10]1[S:9][C:7]2[NH:8][C:2](=[O:1])[CH2:3][N:4]=[C:5]([C:12]3[CH:13]=[CH:14][C:15]([C:16]([O:18][CH3:19])=[O:17])=[CH:20][CH:21]=3)[C:6]=2[CH:11]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24408BromineHCID 136106241(Z)-methyl 4-(2-oxo-2,3-dihydro-1H-thieno[2,3-e][1,4]diazepin-5-yl)benzoate

生成物 1

HCID 136106240(z)-Methyl 4-(7-bromo-2-oxo-2,3-dihydro-1h-thieno[2,3-e][1,4]diazepin-5-yl)benzoate収率 57.2%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
0 °C

実験手順

In a 20 mL dram screw-cap vial with septum was dissolved compound 493 (0.140 g, 0.466 mmol) in pyridine (3 mL) to give an orange solution. The mixture was cooled to 0° C. and bromine (0.029 mL, 0.559 mmol) was added dropwise. The reaction mixture was left to stir at 0° C. for 1 hour. The mixture was quenched with saturated thiosulfate solution and extracted with ethyl acetate. The organic layer was washed several times with water, then brine, dried over magnesium sulfate, filtered and evaporated. The residue was suspended in ether and filtered to afford title compound 494 (101 mg, 57%) as a tan solid. MS (m/z): 379.33 (M+H).

後処理

  1. customIn a 20 mL dram screw-cap vial with septum
  2. customto give an orange solution
  3. waitThe reaction mixture was left
  4. customThe mixture was quenched with saturated thiosulfate solution
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed several times with water
  7. dry with materialbrine, dried over magnesium sulfate
  8. filtrationfiltered
  9. customevaporated
  10. filtrationfiltered

出典と根拠

ORDレコード
ord-cb7ce32af1764a728306eed025037ae9
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399452B2

反応ノート

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