Acetic Acid → HCID 178442980, compound

HRID 151713Notes

Reaction equation

HRID 151713 reaction equation
[CH2:20]([c:21]1[cH:22][cH:23][cH:24][cH:25][cH:26]1)[O:27][C:28](=[O:29])[NH:30][CH:31]([CH:32]([CH3:33])[CH3:34])[C:35](=[O:36])[O:37][CH2:38][CH:39]([CH2:40][C:41](=[O:42])[OH:43])[CH2:44][O:45][C:46]([CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH3:63])=[O:64].[CH3:65][N:66]([c:67]1[cH:68][cH:69][cH:70][cH:71][n:72]1)[CH3:73].[CH3:94][C:95](=[O:96])[OH:97].[CH:74]1([N:75]=[C:76]=[N:77][CH:78]2[CH2:79][CH2:80][CH2:81][CH2:82][CH2:83]2)[CH2:84][CH2:85][CH2:86][CH2:87][CH2:88]1.[Cl:98][CH2:99][Cl:100].[F:1][CH:2]1[CH2:3][CH:4]([n:9]2[cH:10][n:11][c:12]3[c:13](=[O:14])[nH:15][c:16]([NH2:17])[n:18][c:19]23)[O:5][CH:6]1[CH2:7][OH:8].[O:89]=[CH:90][N:91]([CH3:92])[CH3:93]>>[F:1][CH:2]1[CH2:3][CH:4]([n:9]2[cH:10][n:11][c:12]3[c:13](=[O:14])[nH:15][c:16]([NH2:17])[n:18][c:19]23)[O:5][CH:6]1[CH2:7][O:8][C:41]([CH2:40][CH:39]([CH2:38][O:37][C:35]([CH:31]([NH:30][C:28]([O:27][CH2:20][c:21]1[cH:22][cH:23][cH:24][cH:25][cH:26]1)=[O:29])[CH:32]([CH3:33])[CH3:34])=[O:36])[CH2:44][O:45][C:46]([CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH3:63])=[O:64])=[O:42]

Participants

8

Reactant 7

HCID 176Acetic AcidHCID 6228DimethylformamideHCID 6344DichloromethaneHCID 10868DicyclohexylcarbodiimideHCID 218852-DimethylaminopyridineHCID 1355254922-amino-9-[(2R,4R,5R)-4-fluoro-5-(hydroxymethyl)oxolan-2-yl]-6,9-dihydro-1H-purin-6-oneHCID 1784429793-[[3-methyl-2-(phenylmethoxycarbonylamino)butanoyl]oxymethyl]-4-octadecanoyloxybutanoic acid

Product 1

HCID 178442980HCID 178442980, compound

Sources & evidence

ORD record
ord-3a274feaf91f4bddb6651ad2a99f1495
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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