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Acetic Acid → HCID 178502507、化合物

HRID 541554
ノート
印刷プレビュー

反応式

HRID 541554 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 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、化合物

生成物 1

HCID 178502507HCID 178502507、化合物収率 3.7%

試薬・触媒・溶媒 1

HCID 23994Zinc触媒

実験手順

(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.

後処理

  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

出典と根拠

ORDレコード
ord-2b788c461d3c4007b4b1a6a6c68f88fb
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871792B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート