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

HRID 219649노트

반응식

HRID 219649 반응식
[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

참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-f90cbe20e5694c918368c4b052befd9c
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08202863B2

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