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Dimethylformamide → Benzyl 3-(4-t-butoxycarbonylmethoxybenzoyl)carbazate

HRID 1602723
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HRID 1602723 반응식
C[O:2][C:3]([CH2:5][O:6]C1C=CC(C(O)=O)=CC=1)=[O:4].CN(C(ON1N=N[C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][C:25]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C1C=C[C:43]2N(O)N=N[C:44]=2[CH:45]=1.[CH:50](N(C(C)C)CC)(C)C.[C:59]([O:63][CH2:64][C:65]1[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=1)(=[O:62])[NH:60][NH2:61].CN([CH:74]=[O:75])C>>[C:44]([O:4][C:3]([CH2:5][O:6][C:25]1[CH:26]=[CH:27][C:28]([C:74]([NH:61][NH:60][C:59]([O:63][CH2:64][C:65]2[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=2)=[O:62])=[O:75])=[CH:29][CH:30]=1)=[O:2])([CH3:43])([CH3:45])[CH3:50]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 6

HCID 6228DimethylformamideHCID 757711-HydroxybenzotriazoleHCID 79242Benzyl carbazateHCID 81531DiisopropylethylamineHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 138161424-(2-Methoxy-2-oxoethoxy)benzoic acid

생성물 1

HCID 19610493Benzyl 3-(4-t-butoxycarbonylmethoxybenzoyl)carbazate

실험 절차

In a similar manner to Example 9, starting material step (a), 4-methoxycarbonylmethoxybenzoic acid (580 mg), HBTU (1.04 g), HOBT (420 mg), diisopropylethylamine (1.41 ml), DMF (7.5 ml) and benzyl carbazate (500 mg) were reacted to give benzyl 3-(4-t-butoxycarbonylmethoxybenzoyl)carbazate (550 mg) as an off-white solid; NHR Spectrum (DMSO-d6) 3.70 (3H, s), 4.88 (2H, s), 5.11 (2H, s), 7.03 (2H, d), 7.82 (2H, d), 7.38 (5H, m), 9.28 (1H, br s), 10.20 (1H, br s); Mass Spectrum m/z 359 (M+H)+.

후처리

  1. customwere reacted

출처 및 근거

ORD 기록
ord-d96b5b47c6e945a2bf231d2678a98298
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05981531

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