Sulfanilamide → HCID 67428891, compound

HRID 701948Notes

Reaction equation

HRID 701948 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([CH:7]([CH2:8][CH2:9][C:10](=[O:11])[OH:12])[NH:13][C:14](=[O:15])[NH:16][CH:17]([C:18](=[O:19])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])[CH2:25][CH2:26][CH2:27][CH2:28][NH:29][C:30]([c:31]1[cH:32][c:33]([I:37])[cH:34][cH:35][cH:36]1)=[O:38])=[O:39].[CH:75]([N:76]([CH2:77][CH3:78])[CH:79]([CH3:80])[CH3:81])([CH3:82])[CH3:83].[NH2:40][c:41]1[cH:42][cH:43][c:44]([S:47]([NH2:48])(=[O:49])=[O:50])[cH:45][cH:46]1.[O:84]=[CH:85][N:86]([CH3:87])[CH3:88].[P-:51]([F:52])([F:53])([F:54])([F:55])([F:56])[F:57].[n:58]1([O:59][C:60]([N:61]([CH3:62])[CH3:63])=[N+:64]([CH3:65])[CH3:66])[c:67]2[n:68][cH:69][cH:70][cH:71][c:72]2[n:73][n:74]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([CH:7]([CH2:8][CH2:9][C:10](=[O:12])[NH:40][c:41]1[cH:42][cH:43][c:44]([S:47]([NH2:48])(=[O:49])=[O:50])[cH:45][cH:46]1)[NH:13][C:14](=[O:15])[NH:16][CH:17]([C:18](=[O:19])[O:20][C:21]([CH3:22])([CH3:23])[CH3:24])[CH2:25][CH2:26][CH2:27][CH2:28][NH:29][C:30]([c:31]1[cH:32][c:33]([I:37])[cH:34][cH:35][cH:36]1)=[O:38])=[O:39]

Participants

7

Reactant 6

HCID 5333SulfanilamideHCID 6228DimethylformamideHCID 9886HexafluorophosphateHCID 81531DiisopropylethylamineHCID 4641409(Dimethylamino)-N,N-dimethyl(3H-(1,2,3)triazolo(4,5-b)pyridin-3-yloxy)methaniminiumHCID 67442664HCID 67442664, compound

Product 1

HCID 67428891HCID 67428891, compound

Sources & evidence

ORD record
ord-d784037cf0ed485fa6a42aa56e9e65dc
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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