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

Dicyclohexylcarbodiimide → (R)-((R)-quinuclidin-3-yl) 2-(benzyloxycarbonylamino)-2-phenylacetate

HRID 1619514
노트
인쇄 미리보기

반응식

HRID 1619514 반응식
[N:1]12[CH2:8][CH2:7][CH:4]([CH2:5][CH2:6]1)[C@@H:3]([OH:9])[CH2:2]2.C(=NC1CCCCC1)=NC1CCCCC1.N1(O)C2C=CC=CC=2N=N1.[CH2:35]([O:42][C:43]([NH:45][C@H:46]([C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1)[C:47](O)=[O:48])=[O:44])[C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1>C1COCC1>[CH2:35]([O:42][C:43]([NH:45][C@H:46]([C:50]1[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1)[C:47]([O:9][C@@H:3]1[CH:4]2[CH2:7][CH2:8][N:1]([CH2:6][CH2:5]2)[CH2:2]1)=[O:48])=[O:44])[C:36]1[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 10868DicyclohexylcarbodiimideHCID 757711-HydroxybenzotriazoleHCID 87183(R)-(((Phenylmethoxy)carbonyl)amino)phenylacetic acidHCID 914043-Quinuclidinol, (-)-

생성물 1

HCID 67605835(R)-((R)-quinuclidin-3-yl) 2-(benzyloxycarbonylamino)-2-phenylacetate수율 11.4%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

(R)-quinuclidin-3-ol (214 mg, 1.68 mmol), N,N′-methanediylidenedicyclohexanamine (347 mg, 1.68 mmol) and 1H-benzo[d][1,2,3]triazol-1-ol (227 mg, 1.68 mmol) were added to a solution of (R)-2-(benzyloxycarbonylamino)-2-phenylacetic acid (400 mg, 1.40 mmol) in THF (15 ml). The reaction was stirred at RT for 15 hours, and then the solvent was evaporated. DCM was added, and the insoluble solid was removed by filtration. The organic phase was washed twice with Na2CO3 and brine, dried over Na2SO4 and evaporated. The crude was purified by silica gel flash chromatography (DCM/MeOH=9/1) to obtain (R)—((R)-quinuclidin-3-yl) 2-(benzyloxycarbonylamino)-2-phenylacetate (63 mg; 11.4% yield). ((R)-quinuclidin-3-yl 2-(benzyloxycarbonylamino)-2-phenylacetate is also collected (300 mg; 54.2% yield)).

후처리

  1. customthe solvent was evaporated
  2. additionDCM was added
  3. customthe insoluble solid was removed by filtration
  4. washThe organic phase was washed twice with Na2CO3 and brine
  5. dry with materialdried over Na2SO4
  6. customevaporated
  7. customThe crude was purified by silica gel flash chromatography (DCM/MeOH=9/1)

출처 및 근거

ORD 기록
ord-66d20d0178b140d4a00bc49bd424e004
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772314B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트