Acetyl chloride → N-(4-(2-(4-nitronaphthalen-1-yloxy)ethyl)pyridin-2-yl)acetamide

HRID 1774363노트

반응식

HRID 1774363 반응식
[N+:1]([C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]([O:14][CH2:15][CH2:16][C:17]2[CH:22]=[CH:21][N:20]=[C:19]([NH:23]C(=O)OC(C)(C)C)[CH:18]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[C:31](O)([C:33](F)(F)F)=[O:32].CCN(C(C)C)C(C)C.C(Cl)(=O)C>C(Cl)Cl.C([O-])(O)=O.[Na+].C1COCC1>[N+:1]([C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:7]([O:14][CH2:15][CH2:16][C:17]2[CH:22]=[CH:21][N:20]=[C:19]([NH:23][C:31](=[O:32])[CH3:33])[CH:18]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2]

참가 물질

8

반응물 4

HCID 6367Acetyl chlorideHCID 6422Trifluoroacetic acidHCID 81531DiisopropylethylamineHCID 58416756tert-Butyl 4-(2-(4-nitronaphthalen-1-yloxy)ethyl)pyridin-2-ylcarbamate

생성물 1

HCID 67457565N-(4-(2-(4-nitronaphthalen-1-yloxy)ethyl)pyridin-2-yl)acetamide

시약·촉매·용매 3

HCID 6344Dichloromethane용매HCID 8028Tetrahydrofuran용매HCID 516892Sodium Bicarbonate용매

실험 절차

To a suspension of tert-butyl 4-(2-(4-nitronaphthalen-1-yloxy)ethyl)pyridin-2-ylcarbamate (900 mg, 2.20 mmol) in DCM (10.0 mL) was added TFA (10.0 mL) and the reaction mixture was stirred at RT overnight. The resulting mixture was evaporated in vacuo and the residue subjected to SCX capture and release. The crude product so obtained was taken up into THF (8.0 mL) and DIPEA (660 μl, 3.8 mmol) and then acetyl chloride (147 μl, 2.06 mmol) were added. After stirring for 1 hr, the mixture was diluted with saturated aq. NaHCO3 (10.0 mL) and was extracted with EtOAc (2×20 mL). The combined organic layers were washed with brine and then dried, and evaporated in vacuo. The residue was taken up in a mixture of acetonitrile and a solution of NH3 in MeOH (7M, 1:1 v/v, 20 mL) and after 10 min was re-evaporated in vacuo. The residue was triturated with MeOH (10.0 mL) to afford N-(4-(2-(4-nitronaphthalen-1-yloxy)ethyl)pyridin-2-yl)acetamide, as a yellow solid (570 mg, 74%): m/z 352 (M+H)+ (ES+).

후처리

  1. customThe resulting mixture was evaporated in vacuo
  2. customThe crude product so obtained
  3. stirringAfter stirring for 1 hr
  4. extractionwas extracted with EtOAc (2×20 mL)
  5. washThe combined organic layers were washed with brine
  6. customdried
  7. customevaporated in vacuo
  8. additionThe residue was taken up in a mixture of acetonitrile
  9. customa solution of NH3 in MeOH (7M, 1:1 v/v, 20 mL) and after 10 min was re-evaporated in vacuo
  10. customThe residue was triturated with MeOH (10.0 mL)

출처 및 근거

ORD 기록
ord-c39b10fd1d244aa79f1c7965d93bd2a3
출처 데이터셋
uspto-grants-2016_02
특허 번호
US09260410B2

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