Ethylmorpholine → HCID 67806908, 화합물

HRID 1609618노트

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HRID 1609618 반응식
[NH:1]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[C@H:2]([C:4]([OH:6])=O)[CH3:3].C(N1CCOCC1)C.C1C=CC2N(O)N=NC=2C=1.Cl.[CH2:33]([O:40][C:41]([CH:43]1[CH2:51][CH:50]2[CH:45]([CH2:46][CH2:47][CH2:48][CH2:49]2)[NH:44]1)=[O:42])[C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1.C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C=O>[CH2:33]([O:40][C:41]([CH:43]1[CH2:51][CH:50]2[CH:45]([CH2:46][CH2:47][CH2:48][CH2:49]2)[N:44]1[C:4](=[O:6])[C@H:2]([CH3:3])[NH:1][C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])=[O:42])[C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1

참가 물질

7

실험 절차

19 g of Boc-Ala-OH are dissolved in 100 ml of dimethylformamide, and 13 ml of N-ethylmorpholine, 13.5 g of HOBt and 29.6 g of octahydroindole-2-carboxylic acid benzyl ester hydrochloride are added to the solution. The mixture is cooled in an ice bath, 21 g of dicyclohexylcarbodiimide are added to it, and it is stirred for 15 hours at room temperature. The precipitated urea is filtered off under suction, and the filtrate is concentrated in vacuo and taken up in ethyl acetate. The solution is extracted 3 times in each case with aqueous KHSO4 solution, KHCO3 solution and saturated NaCl solution and the organic phase is concentrated in vacuo. Yield: 38.5 g. NMR: 1.26 (d, 3H); 1.40 (s, 9H); 1,1-2,4 (m, 12H); 3.2-3.9 (m, 2H); 5.28 (s, 2H); 7.31 (s, 5H).

후처리

  1. temperatureThe mixture is cooled in an ice bath
  2. filtrationThe precipitated urea is filtered off under suction
  3. concentrationthe filtrate is concentrated in vacuo
  4. extractionThe solution is extracted 3 times in each case with aqueous KHSO4 solution, KHCO3 solution and saturated NaCl solution
  5. concentrationthe organic phase is concentrated in vacuo

출처 및 근거

ORD 기록
ord-66c018cfc7264a1d9ae9b5b3a5408218
출처 데이터셋
uspto-grants-1995_03
특허 번호
US05401766

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