1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 44218281, 화합물

HRID 46008노트

반응식

HRID 46008 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH3:9])[C:6]([S:10]([N:13]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH2:15][C@H:14]2[CH2:22][O:23][CH2:24][C:25]([OH:27])=O)(=[O:12])=[O:11])=[C:5]([CH3:28])[CH:4]=1.C(N(C(C)C)CC)(C)C.C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.Cl.Cl.[CH:61]1([N:64]2[CH2:69][CH2:68][N:67]([C:70]3([CH2:76][NH:77][C:78](=[O:85])[C:79]4[CH:84]=[CH:83][N:82]=[CH:81][CH:80]=4)[CH2:75][CH2:74][NH:73][CH2:72][CH2:71]3)[CH2:66][CH2:65]2)[CH2:63][CH2:62]1>ClCCl.CN(C=O)C>[CH:61]1([N:64]2[CH2:69][CH2:68][N:67]([C:70]3([CH2:76][NH:77][C:78](=[O:85])[C:79]4[CH:80]=[CH:81][N:82]=[CH:83][CH:84]=4)[CH2:75][CH2:74][N:73]([C:25](=[O:27])[CH2:24][O:23][CH2:22][C@@H:14]4[CH2:15][C:16]5[C:21](=[CH:20][CH:19]=[CH:18][CH:17]=5)[N:13]4[S:10]([C:6]4[C:5]([CH3:28])=[CH:4][C:3]([O:2][CH3:1])=[CH:8][C:7]=4[CH3:9])(=[O:11])=[O:12])[CH2:72][CH2:71]3)[CH2:66][CH2:65]2)[CH2:62][CH2:63]1

참가 물질

8

반응물 5

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 57453429HCID 57453429, 화합물HCID 57989597HCID 57989597, 화합물

생성물 1

HCID 44218281HCID 44218281, 화합물수율 58%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 6344Dichloromethane용매2회

반응 조건

온도
0 °C

실험 절차

To a solution of (S)-2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetic acid AC10 (0.282 mmol) in dichloromethane (10 ml/mmol) was added diisopropyl ethylamine (4 equiv.) at 0° C. followed by the addition of HOBT (1.0 equiv.) and EDCI (1.5 equiv.). The resultant solution was stirred at 25° C. for 15 min. It was again cooled to 0° C. and a solution of N-((4-(4-cyclopropyl-piperazin-1-yl)piperidin-4-yl)methyl)isonicotinamide dihydrochloride AM12 (1.2 equiv.) in DMF (2 ml) was added. The reaction mixture was stirred for 16 h at 25° C. The mixture was diluted with dichloromethane, washed with saturated ammonium chloride solution, brine, saturated sodium bicarbonate and finally again with brine. The organic layer was dried over sodium sulfate and evaporated to dryness under reduced pressure to yield the crude product which was purified by column chromatography. Yield: 58%. MS, Rt=3.2 min, m/z=731.5 [MH]+.

후처리

  1. washwashed with saturated ammonium chloride solution, brine, saturated sodium bicarbonate and finally again with brine
  2. dry with materialThe organic layer was dried over sodium sulfate
  3. customevaporated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-c8424830212444c9afd62d74d99a516a
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08541573B2

반응 노트

불러오는 중…