Benzyl Bromide → 2,5-Dibenzyl-4,6-dioxooctahydropyrrolo[3,4-c]pyridine

HRID 1450097ノート

反応式

HRID 1450097 の反応式
C([O-])([O-])=O.[K+].[K+].[CH2:7]([N:14]1[CH2:22][CH:21]2[CH:16]([C:17](=[O:24])[NH:18][C:19](=[O:23])[CH2:20]2)[CH2:15]1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH2:25](Br)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>CN(C=O)C.C(OCC)(=O)C>[CH2:7]([N:14]1[CH2:22][CH:21]2[CH:16]([C:17](=[O:24])[N:18]([CH2:25][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[C:19](=[O:23])[CH2:20]2)[CH2:15]1)[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1

参加物

6

反応物 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 196912212-Benzyl-4,6-dioxooctahydropyrrolo[3.4-c]pyridine

生成物 1

HCID 196913492,5-Dibenzyl-4,6-dioxooctahydropyrrolo[3,4-c]pyridine収率 111.4%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a mixture of 905 mg of K2CO3 and 400 mg of the compound from step 457b in 5 mL of DMF was added 308 mg of benzyl bromide, and the reaction mixture was stirred at room temperature under N2 for 6.5 hours. The mixture was diluted with ethyl acetate, which was washed With water and brine, dried and concentrated to give 610 mg of the title compound.

後処理

  1. washwas washed With water and brine
  2. customdried
  3. concentrationconcentrated

出典と根拠

ORDレコード
ord-28b647207d004655ac5f24cc6638723e
出典データセット
uspto-grants-1997_02
特許番号
US05599816

反応ノート

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