Dimethylformamide → HCID 66855098, compound

HRID 2328759Notes

Reaction equation

HRID 2328759 reaction equation
[CH2:64]([CH3:65])[O:66][C:67](=[O:68])[N:69]1[CH2:70][CH2:71][N:72]([C:75]([CH:76]([CH2:77][CH:78]2[O:79][C:80]([CH3:83])([CH3:84])[O:81][CH2:82]2)[NH2:85])=[O:86])[CH2:73][CH2:74]1.[CH3:92][CH2:93][O:94][C:95](=[O:96])[CH3:97].[CH:1]1([NH:5][C:6](=[O:7])[CH:8]2[N:9]([C:13]([CH2:14][O:15][c:16]3[cH:17][c:18]([C:27](=[O:28])[OH:29])[n:19][n:20]3-[c:21]3[cH:22][cH:23][cH:24][cH:25][cH:26]3)=[O:30])[CH2:10][CH2:11][CH2:12]2)[CH2:2][CH2:3][CH2:4]1.[CH:31]([N:32]([CH2:33][CH3:34])[CH:35]([CH3:36])[CH3:37])([CH3:38])[CH3:39].[O:87]=[CH:88][N:89]([CH3:90])[CH3:91].[P-:40]([F:41])([F:42])([F:43])([F:44])([F:45])[F:46].[n:47]1([O:48][C:49]([N:50]([CH3:51])[CH3:52])=[N+:53]([CH3:54])[CH3:55])[c:56]2[n:57][cH:58][cH:59][cH:60][c:61]2[n:62][n:63]1>>[CH:1]1([NH:5][C:6](=[O:7])[CH:8]2[N:9]([C:13]([CH2:14][O:15][c:16]3[cH:17][c:18]([C:27](=[O:28])[NH:85][CH:76]([C:75]([N:72]4[CH2:71][CH2:70][N:69]([C:67]([O:66][CH2:64][CH3:65])=[O:68])[CH2:74][CH2:73]4)=[O:86])[CH2:77][CH:78]4[O:79][C:80]([CH3:83])([CH3:84])[O:81][CH2:82]4)[n:19][n:20]3-[c:21]3[cH:22][cH:23][cH:24][cH:25][cH:26]3)=[O:30])[CH2:10][CH2:11][CH2:12]2)[CH2:2][CH2:3][CH2:4]1

Participants

8

Reactant 7

HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 9886HexafluorophosphateHCID 81531DiisopropylethylamineHCID 4641409(Dimethylamino)-N,N-dimethyl(3H-(1,2,3)triazolo(4,5-b)pyridin-3-yloxy)methaniminiumHCID 668546965-[2-[2-(Cyclobutylcarbamoyl)pyrrolidin-1-yl]-2-oxoethoxy]-1-phenylpyrazole-3-carboxylic acidHCID 66856139HCID 66856139, compound

Product 1

HCID 66855098HCID 66855098, compound

Sources & evidence

ORD record
ord-476701af3c00430ebbd88706d3699011
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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