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1,2-Dichloroethane → HCID 117996253, 화합물

HRID 1488258
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HRID 1488258 반응식
[CH2:1]([O:8][C:9](=[O:50])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([NH:18][C@H:19]([C:47](O)=[O:48])[CH2:20][CH2:21][CH2:22][CH2:23][NH:24][C:25](=[O:46])[CH2:26][CH2:27][CH2:28][CH2:29][C:30]([NH:32][CH2:33][CH2:34][O:35][C@@H:36]1[O:44][C@@H:43]([CH3:45])[C@@H:41]([OH:42])[C@@H:39]([OH:40])[C@@H:37]1[OH:38])=[O:31])=[O:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(Cl)CCl.C1C=CC2N(O)N=NC=2C=1.[NH2:65][CH2:66][CH2:67][CH2:68][CH2:69][CH2:70][C:71]([NH:73][CH2:74][CH2:75][O:76][C@@H:77]1[O:85][C@@H:84]([CH3:86])[C@@H:82]([OH:83])[C@@H:80]([OH:81])[C@@H:78]1[OH:79])=[O:72]>CN(C=O)C>[C@@H:77]1([O:76][CH2:75][CH2:74][NH:73][C:71](=[O:72])[CH2:70][CH2:69][CH2:68][CH2:67][CH2:66][NH:65][C:47](=[O:48])[C@@H:19]([NH:18][C:16](=[O:17])[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][C:9]([O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)=[O:50])[CH2:20][CH2:21][CH2:22][CH2:23][NH:24][C:25](=[O:46])[CH2:26][CH2:27][CH2:28][CH2:29][C:30](=[O:31])[NH:32][CH2:33][CH2:34][O:35][C@@H:36]2[O:44][C@@H:43]([CH3:45])[C@@H:41]([OH:42])[C@@H:39]([OH:40])[C@@H:37]2[OH:38])[O:85][C@@H:84]([CH3:86])[C@@H:82]([OH:83])[C@@H:80]([OH:81])[C@@H:78]1[OH:79]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 111,2-DichloroethaneHCID 757711-HydroxybenzotriazoleHCID 117995908HCID 117995908, 화합물HCID 117996333HCID 117996333, 화합물

생성물 1

HCID 117996253HCID 117996253, 화합물

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

In a 40 mL vial was added N2-{8-(benzyloxy)-8-oxooctanoyl}-N6-[6-({2-[(α-L-fucopyranosyl)oxy]ethyl}amino)-6-oxohexanoyl]-L-lysine (100 mg, 0.141 mmol) and DMF (5 mL). To the above solution at 0° C. was added EDC (40.5 mg, 0.211 mmol) and HOBt (23.7 mg, 0.155 mmol). The reaction was warmed to rt and stirred at rt for 20 min. To the above mixture was added 6-amino-N-{2-[(α-L-fucopyranosyl)oxy]ethyl}hexanamide (45.1 mg, 0.141 mmol). After stirring at rt for 18 hr, the mixture was concentrated. The residue was purified by flash chromatography eluting with 0-40% AcCN in water to give the title compound. UPLC Method B: m/e=1012.6348 [M+1]; Rt=3.28 min.

후처리

  1. stirringAfter stirring at rt for 18 hr
  2. concentrationthe mixture was concentrated
  3. customThe residue was purified by flash chromatography
  4. washeluting with 0-40% AcCN in water

출처 및 근거

ORD 기록
ord-4f42af457a41466f8e25a33feda683bd
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09427475B2

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