Sodium cyanoborohydride → 2-(2-Pyrrolidin-1-yl-ethyl)-benzooxazol-6-ylamine

HRID 219649ノート

反応式

HRID 219649 の反応式
[N:1]1([CH:6]=[CH:7][C:8]2[O:9][C:10]3[CH:16]=[C:15]([NH2:17])[CH:14]=[CH:13][C:11]=3[N:12]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1.C([BH3-])#N.[Na+]>CO>[N:1]1([CH2:6][CH2:7][C:8]2[O:9][C:10]3[CH:16]=[C:15]([NH2:17])[CH:14]=[CH:13][C:11]=3[N:12]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1

参加物

4

反応物 2

HCID 5003444Sodium cyanoborohydrideHCID 866232152-(2-Pyrrolidin-1-yl-vinyl)-benzooxazol-6-ylamine

生成物 1

HCID 691228932-(2-Pyrrolidin-1-yl-ethyl)-benzooxazol-6-ylamine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 2-(2-pyrrolidin-1-yl-vinyl)-benzooxazol-6-ylamine (3.2 mmol) in MeOH (40 mL) is added sodium cyanoborohydride (6.4 mmol) at room temperature. The reaction mixture is heated to reflux for 18 hours. The mixture is concentrated and the residue is dissolved in DCM. The solution is washed with water and brine, and dried (MgSO4). A small amount of activated carbon is added to the solution, and the mixture is filtered. The filtrate is concentrated to afford 2-(2-pyrrolidin-1-yl-ethyl)-benzooxazol-6-ylamine as a solid. 1H NMR (300 MHz, CDCl3): δ 1.79 (m, 4H), 2.61 (m, 4H), 3.00-3.18 (m, 4H), 4.78 (broad, 2N—H), 6.68 (q, H), 6.80 (d, H), 7.43 (d, H).

後処理

  1. temperatureThe reaction mixture is heated
  2. temperatureto reflux for 18 hours
  3. concentrationThe mixture is concentrated
  4. dissolutionthe residue is dissolved in DCM
  5. washThe solution is washed with water and brine
  6. dry with materialdried (MgSO4)
  7. additionA small amount of activated carbon is added to the solution
  8. filtrationthe mixture is filtered
  9. concentrationThe filtrate is concentrated

出典と根拠

ORDレコード
ord-f90cbe20e5694c918368c4b052befd9c
出典データセット
uspto-grants-2012_06
特許番号
US08202863B2

反応ノート

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