홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

4-Amino-1,2,2,6,6-pentamethylpiperidine → 4-(5,6-Dichlorobenzimidazol-2-yl)-N-(1,2,2,6,6-pentamethylpiperidin-4-yl)-3-methoxybenzamide

HRID 1352665
노트
인쇄 미리보기

반응식

HRID 1352665 반응식
[Cl:1][C:2]1[C:21]([Cl:22])=[CH:20][C:5]2[N:6]=[C:7]([C:9]3[CH:14]=[CH:13][C:12]([C:15](O)=[O:16])=[CH:11][C:10]=3[O:18][CH3:19])[NH:8][C:4]=2[CH:3]=1.Cl.CN(C)CCCN=C=NCC.[CH3:35][N:36]1[C:41]([CH3:43])([CH3:42])[CH2:40][CH:39]([NH2:44])[CH2:38][C:37]1([CH3:46])[CH3:45]>CN(C=O)C.C1COCC1.C1COCC1>[Cl:1][C:2]1[C:21]([Cl:22])=[CH:20][C:5]2[N:6]=[C:7]([C:9]3[CH:14]=[CH:13][C:12]([C:15]([NH:44][CH:39]4[CH2:38][C:37]([CH3:45])([CH3:46])[N:36]([CH3:35])[C:41]([CH3:43])([CH3:42])[CH2:40]4)=[O:16])=[CH:11][C:10]=3[O:18][CH3:19])[NH:8][C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6937924-Amino-1,2,2,6,6-pentamethylpiperidineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 211011665,6-Dichloro-2-(4-carboxy-2-methoxyphenyl)benzimidazole

생성물 1

HCID 99134174-(5,6-Dichlorobenzimidazol-2-yl)-N-(1,2,2,6,6-pentamethylpiperidin-4-yl)-3-methoxybenzamide수율 47.6%

시약·촉매·용매 2

HCID 8028
Tetrahydrofuran
용매
HCID 21974620tetrahydrofuran N,N-dimethylformamide용매

실험 절차

A solution of 5,6-dichloro-2-(4-carboxy-2-methoxyphenyl)benzimidazole (0.8 g, 2,36 mmol), prepared as described in Preparation 6,1-hydroxybenzotriazole (0.32 g, 2.36 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.56 g, 2.9 mmol) in 80 ml of DMF/THF (50:50) was refluxed for 5 h. A solution of 1,2,2,6,6-pentamethyl-4-aminopiperidine (0.5 g, 2.9 mmol) in THF (5 ml) was added dropwise and the reaction was refluxed for additional 3 h. After cooling, solvent was removed under reduced pressure and the residue was treated with 1N NaOH (10 ml) and extracted with dichloromethane (50 ml). The organic layer was washed with water, dried over Na2SO4, filtered and evaporated under reduced pressure. The residue was triturated with diisopropyl ether (150 ml), stirred for 1 h, filtered to give 0.55 g of the title compound (yield 47.6%), mp=285–286° C.

후처리

  1. temperaturewas refluxed for 5 h
  2. temperaturethe reaction was refluxed for additional 3 h
  3. temperatureAfter cooling
  4. customsolvent was removed under reduced pressure
  5. additionthe residue was treated with 1N NaOH (10 ml)
  6. extractionextracted with dichloromethane (50 ml)
  7. washThe organic layer was washed with water
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. customevaporated under reduced pressure
  11. customThe residue was triturated with diisopropyl ether (150 ml)
  12. filtrationfiltered

출처 및 근거

ORD 기록
ord-af7ad8f0a1dc42b390a8d59218c54b8b
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07220769B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트