Dimethyl Sulfoxide → HCID 67041161, compound

HRID 175630Notes

Reaction equation

HRID 175630 reaction equation
[B-:39]([F:40])([F:41])([F:42])[F:43].[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][c:9]1[cH:10][cH:11][c:12]([S:15][c:16]2[c:17]([NH:25][c:26]3[c:27]4[c:28]([n:29][cH:30][n:31]3)[n:32][c:33]([CH:36]([CH3:37])[CH3:38])[cH:34][cH:35]4)[cH:18][c:19]([C:20](=[O:21])[OH:22])[cH:23][cH:24]2)[cH:13][cH:14]1.[CH3:88][S:89]([CH3:90])=[O:91].[CH3:92][CH2:93][O:94][C:95](=[O:96])[CH3:97].[CH:79]([N:80]([CH2:81][CH3:82])[CH:83]([CH3:84])[CH3:85])([CH3:86])[CH3:87].[P:61](=[O:62])([O:63][CH2:64][C:65]([CH3:66])([CH3:67])[NH2:68])([O:69][C:70]([CH3:71])([CH3:72])[CH3:73])[O:74][C:75]([CH3:76])([CH3:77])[CH3:78].[n:44]1([O:45][C:46]([N:47]([CH3:48])[CH3:49])=[N+:50]([CH3:51])[CH3:52])[c:53]2[cH:54][cH:55][cH:56][cH:57][c:58]2[n:59][n:60]1>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[NH:8][c:9]1[cH:10][cH:11][c:12]([S:15][c:16]2[c:17]([NH:25][c:26]3[c:27]4[c:28]([n:29][cH:30][n:31]3)[n:32][c:33]([CH:36]([CH3:37])[CH3:38])[cH:34][cH:35]4)[cH:18][c:19]([C:20](=[O:21])[NH:68][C:65]([CH2:64][O:63][P:61](=[O:62])([O:69][C:70]([CH3:71])([CH3:72])[CH3:73])[O:74][C:75]([CH3:76])([CH3:77])[CH3:78])([CH3:66])[CH3:67])[cH:23][cH:24]2)[cH:13][cH:14]1

Participants

8

Reactant 7

HCID 679Dimethyl SulfoxideHCID 8857Ethyl AcetateHCID 26255TetrafluoroborateHCID 81531DiisopropylethylamineHCID 130500O-benzotriazol-1-yl-tetramethyluroniumHCID 593768924-(4-tert-Butoxycarbonylamino-phenylsulfanyl)-3-(7-isopropyl-pyrido[2,3-d]pyrimidin-4-ylamino)-benzoic acidHCID 866155662-Amino-2-methylpropyl di-tert-butyl phosphate

Product 1

HCID 67041161HCID 67041161, compound

Sources & evidence

ORD record
ord-5780b61977824109aa12efd8317aff91
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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