Ethylmorpholine → N-{2-(4-Chlorophenyl)-1-[(2,2-diethoxyethyl)isopropylcarbamoyl]ethyl}-3-(2,4-dichlorobenzenesulfonylamino)-2-methanesulfonylaminopropionamide

HRID 1670499노트

반응식

HRID 1670499 반응식
C1C=CC2N(O)N=NC=2C=1.C(N1CCOCC1)C.C(OC([NH:29][CH:30]([CH2:34][NH:35][S:36]([C:39]1[CH:44]=[CH:43][C:42]([Cl:45])=[CH:41][C:40]=1[Cl:46])(=[O:38])=[O:37])[C:31]([OH:33])=O)=O)C1C=CC=CC=1.[NH2:47][CH:48]([CH2:63][C:64]1[CH:69]=[CH:68][C:67]([Cl:70])=[CH:66][CH:65]=1)[C:49]([N:51]([CH2:55][CH:56]([O:60][CH2:61][CH3:62])[O:57][CH2:58][CH3:59])[CH:52]([CH3:54])[CH3:53])=[O:50]>CN(C=O)C.C(Cl)CCl>[Cl:70][C:67]1[CH:66]=[CH:65][C:64]([CH2:63][CH:48]([NH:47][C:31](=[O:33])[CH:30]([NH:29][S:36]([CH3:39])(=[O:38])=[O:37])[CH2:34][NH:35][S:36]([C:39]2[CH:44]=[CH:43][C:42]([Cl:45])=[CH:41][C:40]=2[Cl:46])(=[O:37])=[O:38])[C:49](=[O:50])[N:51]([CH2:55][CH:56]([O:60][CH2:61][CH3:62])[O:57][CH2:58][CH3:59])[CH:52]([CH3:54])[CH3:53])=[CH:69][CH:68]=1

참가 물질

7

반응물 4

HCID 7525EthylmorpholineHCID 757711-HydroxybenzotriazoleHCID 673394042-Benzyloxycarbonylamino-3-(2,4-dichlorobenzenesulfonylamino)propionic acidHCID 673416462-amino-3-(4-chlorophenyl)-N-(2,2-diethoxyethyl)-N-isopropylpropionamide

생성물 1

HCID 67340421N-{2-(4-Chlorophenyl)-1-[(2,2-diethoxyethyl)isopropylcarbamoyl]ethyl}-3-(2,4-dichlorobenzenesulfonylamino)-2-methanesulfonylaminopropionamide

시약·촉매·용매 2

HCID 111,2-Dichloroethane용매HCID 6228Dimethylformamide용매2회

실험 절차

52 mg of EDC, 45 mg of HOBt and 100 μl of N-ethylmorpholine are added to a solution of 124 mg of 2-benzyloxycarbonylamino-3-(2,4-dichlorobenzenesulfonylamino)propionic acid in 1 ml of DMF. A solution of 100 mg of 2-amino-3-(4-chlorophenyl)-N-(2,2-diethoxyethyl)-N-isopropylpropionamide in 1 ml of DMF is added dropwise thereto, and the solution is left to stir for 12 h. The reaction solution is filtered, mixed with ethyl acetate and then extracted with 5% aqueous sodium bicarbonate solution and aqueous sodium chloride solution. Drying of the organic phase over sodium sulfate is followed by concentration under reduced pressure, and the residue is separated by HPLC (Knauer Eurospher-100-10-C18, water (0.1% trifluoroacetic acid)/acetonitrile (0.1% trifluoroacetic acid)=80/20→10/90). The desired product is obtained with MW=784.186 (calculated); measured value (M−CO2+H)+: 741.10.

후처리

  1. waitthe solution is left
  2. filtrationThe reaction solution is filtered
  3. additionmixed with ethyl acetate
  4. extractionextracted with 5% aqueous sodium bicarbonate solution and aqueous sodium chloride solution
  5. dry with materialDrying of the organic phase over sodium sulfate
  6. concentrationis followed by concentration under reduced pressure
  7. customthe residue is separated by HPLC (Knauer Eurospher-100-10-C18, water (0.1% trifluoroacetic acid)/acetonitrile (0.1% trifluoroacetic acid)=80/20→10/90)

출처 및 근거

ORD 기록
ord-682df87d12e9445f95ee9c28342716ee
출처 데이터셋
uspto-grants-2011_08
특허 번호
US07994168B2

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