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Methylamine → HCID 90408407、化合物

HRID 594038
ノート
印刷プレビュー

反応式

HRID 594038 の反応式
[CH3:1][NH2:2].CC1C=CC(S(O[CH2:14][C@H:15]2[O:20][CH2:19][CH2:18][N:17]([C:21]3[CH:26]=[C:25]([Br:27])[CH:24]=[CH:23][N:22]=3)[CH2:16]2)(=O)=O)=CC=1>CO>[Br:27][C:25]1[CH:24]=[CH:23][N:22]=[C:21]([N:17]2[CH2:18][CH2:19][O:20][C@H:15]([CH2:14][NH:2][CH3:1])[CH2:16]2)[CH:26]=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 6329MethylamineHCID 90409573HCID 90409573、化合物

生成物 1

HCID 90408407HCID 90408407、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
80 °C

実験手順

To a 2 M solution of methylamine in methanol was added (S)-(4-(4-bromopyridin-2-yl)morpholin-2-yl)methyl 4-methylbenzenesulfonate (1.0 eq). This solution was microwave heated at 80° C. After 1 h the solution was then concentrated in vacuo and water was added. The resulting suspension was sonicated and centrifuged. The water soluble portion was separated from the solids. The resulting aqueous solution of (R)-1-(4-(4-bromopyridin-2-yl)morpholin-2-yl)-N-methylmethanamine was used in the next step without further purification. LCMS (m/z) (M+H)=286.0/288.0, Rt=0.34 min.

後処理

  1. concentrationAfter 1 h the solution was then concentrated in vacuo and water
  2. additionwas added
  3. customThe resulting suspension was sonicated
  4. customThe water soluble portion was separated from the solids
  5. customThe resulting aqueous solution of (R)-1-(4-(4-bromopyridin-2-yl)morpholin-2-yl)-N-methylmethanamine was used in the next step without further purification

出典と根拠

ORDレコード
ord-e14b19294da74389b8ce128879895998
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242969B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート