[(2S,3S,4S,5R,6S)-6-bromo-3,4,5-tris(2,2-dimethylpropanoyloxy)tetrahydropyran-2-yl]methyl 2,2-dimethylpropanoate → HCID 178440281, compound

HRID 2322833Notes

Reaction equation

HRID 2322833 reaction equation
[C:32]([C:33]([CH3:34])([CH3:35])[CH3:36])(=[O:37])[O:38][CH:39]1[CH:40]([Br:67])[O:41][CH:42]([CH2:59][O:60][C:61]([C:62]([CH3:63])([CH3:64])[CH3:65])=[O:66])[CH:43]([O:52][C:53]([C:54]([CH3:55])([CH3:56])[CH3:57])=[O:58])[CH:44]1[O:45][C:46]([C:47]([CH3:48])([CH3:49])[CH3:50])=[O:51].[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][c:9]1[cH:10][c:11]([O:25][CH:26]2[CH2:27][CH2:28][O:29][CH2:30][CH2:31]2)[c:12]([CH2:15][c:16]2[c:17](=[O:24])[nH:18][nH:19][c:20]2[CH:21]([CH3:22])[CH3:23])[cH:13][cH:14]1>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[O:8][c:9]1[cH:10][c:11]([O:25][CH:26]2[CH2:27][CH2:28][O:29][CH2:30][CH2:31]2)[c:12]([CH2:15][c:16]2[c:17]([O:24][CH:40]3[CH:39]([O:38][C:32]([C:33]([CH3:34])([CH3:35])[CH3:36])=[O:37])[CH:44]([O:45][C:46]([C:47]([CH3:48])([CH3:49])[CH3:50])=[O:51])[CH:43]([O:52][C:53]([C:54]([CH3:55])([CH3:56])[CH3:57])=[O:58])[CH:42]([CH2:59][O:60][C:61]([C:62]([CH3:63])([CH3:64])[CH3:65])=[O:66])[O:41]3)[n:18][nH:19][c:20]2[CH:21]([CH3:22])[CH3:23])[cH:13][cH:14]1

Participants

3

Reactant 2

HCID 14583857[(2S,3S,4S,5R,6S)-6-bromo-3,4,5-tris(2,2-dimethylpropanoyloxy)tetrahydropyran-2-yl]methyl 2,2-dimethylpropanoateHCID 685376674-{[4-benzyloxy-2-(tetrahydro-4H-pyran-4-yloxy)phenyl]methyl}-1,2-dihydro-5-isopropyl-3H-pyrazol-3-one

Product 1

HCID 178440281HCID 178440281, compound

Sources & evidence

ORD record
ord-a99e883fffbc44eba9b82abc2395e010
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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