ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Hydrochloric Acid → 3-Pyridinemethanamine,2-(methylamino)-(9CI)

HRID 1723021
ノート
印刷プレビュー

反応式

HRID 1723021 の反応式
[CH3:1][NH:2][C:3]1[N:10]=[CH:9][CH:8]=[CH:7][C:4]=1[C:5]#[N:6].CO.Cl>O1CCCC1>[NH2:6][CH2:5][C:4]1[C:3]([NH:2][CH3:1])=[N:10][CH:9]=[CH:8][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric Acid2 回HCID 887MethanolHCID 124571912-(Methylamino)pyridine-3-carbonitrile

生成物 1

HCID 145183013-Pyridinemethanamine,2-(methylamino)-(9CI)収率 68.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Borane/THF complex (1.44 mol) as a 1M solution in tetrahydrofuran was added, dropwise, to a solution of 2-(methylamino)-nicotinonitrile (63.9 g, 480 mmol) in tetrahydrofuran (480 mL). This mixture was stirred at room temperature for 1 hour then heated to reflux for 3 hours. The reaction mixture was quenched by dropwise addition of methanol (136 mL, 3.36 mol) followed by 6M HCl (80 mol, 480 mmol) and 10% HCl (400 mL). The phases were separated and the organic phase washed with brine (2×480 mL). The aqueous phase was made alkaline with 50% aqueous NaOH (250 g). The aqueous phase was extracted with dichloromethane (2×480 mL) and the organic extracts dried over Na2SO4. Concentration in vacuo gave 44.85 g of 3-(aminomethyl)-2-methylaminopyridine as a pale yellow oil.

後処理

  1. temperaturethen heated
  2. temperatureto reflux for 3 hours
  3. customThe phases were separated
  4. washthe organic phase washed with brine (2×480 mL)
  5. extractionThe aqueous phase was extracted with dichloromethane (2×480 mL)
  6. dry with materialthe organic extracts dried over Na2SO4
  7. concentrationConcentration in vacuo

出典と根拠

ORDレコード
ord-688fb188921f41a0be0c1c272541d206
出典データセット
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04859672

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート