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

Phenethylamine → Pyrrolidine-1-carboxylic acid 4-phenethylcarbamoyloxy-cyclohexylmethyl ester

HRID 68483
노트
인쇄 미리보기

반응식

HRID 68483 반응식
[OH:1][CH2:2][CH:3]1[CH2:8][CH2:7][CH:6]([OH:9])[CH2:5][CH2:4]1.C1N=CN([C:15]([N:17]2[CH:21]=N[CH:19]=[CH:18]2)=[O:16])C=1.N1CCCC1.[CH3:27]I.[CH2:29]([NH2:37])[CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1.[O:38]1CCC[CH2:39]1>O.C(#N)C>[CH2:29]([NH:37][C:39]([O:9][CH:6]1[CH2:7][CH2:8][CH:3]([CH2:2][O:1][C:15]([N:17]2[CH2:18][CH2:19][CH2:27][CH2:21]2)=[O:16])[CH2:4][CH2:5]1)=[O:38])[CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 6

HCID 1001PhenethylamineHCID 6328Methyl iodideHCID 8028TetrahydrofuranHCID 31268PyrrolidineHCID 682631,1'-Carbonyldiimidazole2회HCID 12892866Rac-(1s,4s)-4-(hydroxymethyl)cyclohexanol

생성물 1

HCID 56953266
Pyrrolidine-1-carboxylic acid 4-phenethylcarbamoyloxy-cyclohexylmethyl ester
수율 55%

시약·촉매·용매 2

HCID 962Water용매2회HCID 6342Acetonitrile용매

실험 절차

To a solution of 4-hydroxymethylcyclohexanol (2 mmol) in 10 mL of tetrahydrofuran (THF) was added CDI (2.2 mmol) and the resulting mixture was stirred for 2 hours at room temperature. Then, pyrrolidine (3 mmol) was added and stirred for 2 hours at 60° C. The reaction mixture was diluted with water, followed by few times of extraction with methylene chloride. The combined organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, hexane:ethyl acetate=1:1) to provide a intermediate compound. The intermediate compound was dissolved in acetonitrile (10 mL), and CDI (2.2 mmol) was added. After 1 hour stirring at 80° C., methyl iodide (10 mmol) was added and stirred for additional 1 hour at 80° C. The resulting reaction mixture was concentrated under reduced pressure. The residue was dissolved in acetonitrile (10 mL), and phenethylamine (3 mmol) was added and stirred for 4 hours at 80° C. The reaction mixture was diluted with water, followed by few times of extraction with methylene chloride. The combined organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, hexane:ethyl acetate=1:3), thereby completing the preparation of a target compound (411 mg, 55% yield).

후처리

  1. stirringstirred for 2 hours at 60° C
  2. extractionfollowed by few times of extraction with methylene chloride
  3. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by column chromatography (silica gel, hexane:ethyl acetate=1:1)
  7. customto provide a intermediate compound
  8. stirringAfter 1 hour stirring at 80° C.
  9. stirringstirred for additional 1 hour at 80° C
  10. customThe resulting reaction mixture
  11. concentrationwas concentrated under reduced pressure
  12. dissolutionThe residue was dissolved in acetonitrile (10 mL)
  13. stirringstirred for 4 hours at 80° C
  14. extractionfollowed by few times of extraction with methylene chloride
  15. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  16. filtrationfiltered
  17. concentrationconcentrated under reduced pressure
  18. customThe residue was purified by column chromatography (silica gel, hexane:ethyl acetate=1:3)

출처 및 근거

ORD 기록
ord-0a11e633b30447f1beaaca692222b610
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822463B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트