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Acetic Acid → HCID 178502507, 화합물

HRID 541554
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HRID 541554 반응식
[CH3:1][O:2][C:3]([NH:5][C@@H:6]([CH:10]([CH3:12])[CH3:11])[C:7]([OH:9])=[O:8])=[O:4].CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(Cl)Cl.O=C(C1C=CC=CC=1)C[O:43][C:44](=[O:72])[C@H:45](O)[CH2:46][N:47]([CH2:57][C:58]1[CH:63]=[CH:62][C:61]([C:64]2[CH:69]=[CH:68][CH:67]=[C:66]([Cl:70])[CH:65]=2)=[CH:60][CH:59]=1)[NH:48][C:49]([C:51]1[O:55][N:54]=[C:53]([OH:56])[CH:52]=1)=[O:50].CCN(C(C)C)C(C)C.CC(O)=O>[Zn]>[C:44]([C@H:45]([O:8][C:7](=[O:9])[C@@H:6]([NH:5][C:3]([O:2][CH3:1])=[O:4])[CH:10]([CH3:12])[CH3:11])[CH2:46][N:47]([CH2:57][C:58]1[CH:63]=[CH:62][C:61]([C:64]2[CH:69]=[CH:68][CH:67]=[C:66]([Cl:70])[CH:65]=2)=[CH:60][CH:59]=1)[NH:48][C:49]([C:51]1[O:55][N:54]=[C:53]([OH:56])[CH:52]=1)=[O:50])([OH:72])=[O:43]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 176Acetic AcidHCID 6344DichloromethaneHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 10942966(2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acidHCID 178521475HCID 178521475, 화합물

생성물 1

HCID 178502507HCID 178502507, 화합물수율 3.7%

시약·촉매·용매 1

HCID 23994Zinc촉매

실험 절차

(S)-2-Methoxycarbonylamino-3-methylbutyric acid (9.6 mg, 54.5 μmol) and HATU (23.5 mg, 62 μmol) were stirred in DCM (1.0 mL, 16 mmol) for 10 minutes. (R)-3-[N-(3′-Chlorobiphenyl-4-ylmethyl)-N′-(3-hydroxyisoxazole-5-carbonyl)hydrazino]-2-hydroxypropionic acid 2-oxo-2-phenylethyl ester (20.0 mg, 36.4 μmol) and DIPEA (31.7 μL, 182 μmol) were added, and the resulting mixture was stirred at room temperature overnight. The mixture was then concentrated and purified by flash chromatography (EtOAc/hexanes=0-100%). Zinc (119 mg, 1.8 mmol) and AcOH (0.5 mL, 9 mmol) were added. The mixture was stirred for 2 hours and filtered. The solids were washed with AcOH (1 mL) and filtered. The combined filtrates were purified by reverse phase preparative HPLC to yield the title compound (0.8 mg). MS m/z [M+H]+ calc'd for C27H29ClN4O9, 589.16. found 589.3.

후처리

  1. concentrationThe mixture was then concentrated
  2. custompurified by flash chromatography (EtOAc/hexanes=0-100%)
  3. stirringThe mixture was stirred for 2 hours
  4. filtrationfiltered
  5. washThe solids were washed with AcOH (1 mL)
  6. filtrationfiltered
  7. customThe combined filtrates were purified by reverse phase preparative HPLC

출처 및 근거

ORD 기록
ord-2b788c461d3c4007b4b1a6a6c68f88fb
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871792B2

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