Tetrahydrofuran → 2,6-Dichloro-9-(tetrahydro-2H-pyran-4-ylmethyl)-9H-purine

HRID 210269

Reaction equation

HRID 210269 reaction equation
[CH2:53]1[O:54][CH2:55][CH2:56][CH2:57]1.[Cl:9][c:10]1[n:11][c:12]([Cl:19])[c:13]2[nH:14][cH:15][n:16][c:17]2[n:18]1.[O:1]1[CH2:2][CH2:3][CH:4]([CH2:7][OH:8])[CH2:5][CH2:6]1.[O:39]=[C:40]([O:41][CH:42]([CH3:43])[CH3:44])[N:45]=[N:46][C:47]([O:48][CH:49]([CH3:50])[CH3:51])=[O:52].[c:20]1([P:21]([c:22]2[cH:23][cH:24][cH:25][cH:26][cH:27]2)[c:28]2[cH:29][cH:30][cH:31][cH:32][cH:33]2)[cH:34][cH:35][cH:36][cH:37][cH:38]1>>[O:1]1[CH2:2][CH2:3][CH:4]([CH2:7][n:16]2[cH:15][n:14][c:13]3[c:12]([Cl:19])[n:11][c:10]([Cl:9])[n:18][c:17]32)[CH2:5][CH2:6]1

Participants

6

Reactant 5

HCID 8028TetrahydrofuranHCID 11776TriphenylphosphineHCID 75555Diisopropyl diazene-1,2-dicarboxylateHCID 2773573(Oxan-4-yl)methanolHCID 53244122,6-Dichloropurine

Product 1

HCID 576997032,6-Dichloro-9-(tetrahydro-2H-pyran-4-ylmethyl)-9H-purine

Sources & evidence

ORD record
ord-3d2f0d10cd684f06a81d90e9d374fdaf
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Linked notes

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