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Dicyclohexylcarbodiimide → HCID 15614978, 화합물

HRID 620225
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HRID 620225 반응식
[CH2:1]1[C:9]2[C:4](=[CH:5][C:6]([NH:10][CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.C1(N=C=NC2CCCCC2)CCCCC1.[C:32]([NH:42][C@H:43]([C:45](O)=[O:46])[CH3:44])([O:34][CH2:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)=[O:33]>C(Cl)Cl>[C:32]([NH:42][C@H:43]([C:45]([N:10]([C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[CH2:1][CH2:2][CH2:3]2)[CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])=[O:46])[CH3:44])([O:34][CH2:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)=[O:33]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10868DicyclohexylcarbodiimideHCID 736104N-carbobenzyloxyalanineHCID 15614976Ethyl N-(2,3-dihydro-1H-inden-5-yl)glycinate

생성물 1

HCID 15614978HCID 15614978, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of ethyl N-(5-indanyl)-glycinate (10.6 g, 48.4 mmol) and N,N'-dicyclohexylcarbodiimide (10.5 g, 50.8 mmol) in 200 ml CH2Cl2 at 0° C. was added dropwise a solution of N-carbobenzyloxy-L-alanine (11.3 g, 50.8 mmol) in 100 ml CH2Cl2. After the addition was completed the solution was stirred 10 min., warmed to room temperature and stirred overnight. The solution was filtered and concentrated in vacuo. The residue was dissolved in ether, filtered, washed with saturated NaHCO3, 10% aqueous HCl (5x), brine and dried MgSO4). Concentration of the volatiles in vacuo provided the product.

후처리

  1. additionAfter the addition
  2. stirringstirred overnight
  3. filtrationThe solution was filtered
  4. concentrationconcentrated in vacuo
  5. dissolutionThe residue was dissolved in ether
  6. filtrationfiltered
  7. washwashed with saturated NaHCO3, 10% aqueous HCl (5x), brine and dried MgSO4)
  8. customConcentration of the volatiles in vacuo provided the product

출처 및 근거

ORD 기록
ord-77c0d499d4224b3299ab81c279511935
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04820729

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