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4-Aminocarbonylphenylboronic acid → HCID 46846504, 화합물

HRID 2114454
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HRID 2114454 반응식
[Cl:1][C:2]1[C:3]([Cl:40])=[CH:4][C:5]2[O:10][CH2:9][C:8](=[O:11])[N:7]([CH2:12][C:13]([N:15]([CH3:38])[C@H:16]([C:23]3[CH:28]=[CH:27][C:26](C4C=CC=C(C(N)=O)C=4)=[CH:25][CH:24]=3)[CH2:17][N:18]3[CH2:22][CH2:21][CH2:20][CH2:19]3)=[O:14])[C:6]=2[CH:39]=1.[NH2:41][C:42]([C:44]1[CH:49]=[CH:48][C:47](B(O)O)=[CH:46][CH:45]=1)=[O:43]>>[Cl:1][C:2]1[C:3]([Cl:40])=[CH:4][C:5]2[O:10][CH2:9][C:8](=[O:11])[N:7]([CH2:12][C:13]([N:15]([CH3:38])[C@H:16]([C:23]3[CH:24]=[CH:25][C:26]([C:47]4[CH:48]=[CH:49][C:44]([C:42]([NH2:41])=[O:43])=[CH:45][CH:46]=4)=[CH:27][CH:28]=3)[CH2:17][N:18]3[CH2:19][CH2:20][CH2:21][CH2:22]3)=[O:14])[C:6]=2[CH:39]=1
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3

반응물 2

HCID 27378114-Aminocarbonylphenylboronic acidHCID 46846503N-[(1R)-1-[3′-(Aminocarbonyl)[1,1′-biphenyl]-4-yl]-2-(1-pyrrolidinyl)ethyl]-6,7-dichloro-2,3-dihydro-N-methyl-3-oxo-4H-1,4-benzoxazine-4-acetamide

생성물 1

HCID 46846504HCID 46846504, 화합물

실험 절차

4′-[(1R)-1-[[(6,7-dichloro-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)acetyl](methyl)amino]-2-(1-pyrrolidinyl)ethyl]-4-biphenylcarboxamide was prepared in a similar manner as in the preparation of 4′-[(1R)-1-[[(6,7-dichloro-3-oxo-2,3-dihydro-4H-1,4-benzoxazin-4-yl)acetyl](methyl)amino]-2-(1-pyrrolidinyl)ethyl]-3-biphenylcarboxamide except replacing [3-(aminocarbonyl)phenyl]boronic acid with [4-(aminocarbonyl)phenyl]boronic acid. As is appreciated by those skilled in the art, this analogous example may involve variations in synthetic procedure.

출처 및 근거

ORD 기록
ord-9c522f05037e46b3b389280d71885b95
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07432258B2

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