Tetrahydrofuran → 6-Chloro-9-[4-di(propan-2-yloxy)phosphorylbut-3-enyl]purine

HRID 133905

Reaction equation

HRID 133905 reaction equation
[Cl:1][c:2]1[c:3]2[nH:4][cH:5][n:6][c:7]2[n:8][cH:9][n:10]1.[O:45]=[C:46]([O:47][CH2:48][CH3:49])[N:50]=[N:51][C:52]([O:53][CH2:54][CH3:55])=[O:56].[O:57]1[CH2:58][CH2:59][CH2:60][CH2:61]1.[OH:11][CH2:12][CH2:13][CH:14]=[CH:15][P:16]([O:17][CH:18]([CH3:19])[CH3:20])([O:21][CH:22]([CH3:23])[CH3:24])=[O:25].[c:26]1([P:27]([c:28]2[cH:29][cH:30][cH:31][cH:32][cH:33]2)[c:34]2[cH:35][cH:36][cH:37][cH:38][cH:39]2)[cH:40][cH:41][cH:42][cH:43][cH:44]1>>[Cl:1][c:2]1[c:3]2[n:4][cH:5][n:6]([CH2:12][CH2:13][CH:14]=[CH:15][P:16]([O:17][CH:18]([CH3:19])[CH3:20])([O:21][CH:22]([CH3:23])[CH3:24])=[O:25])[c:7]2[n:8][cH:9][n:10]1

Participants

6

Reactant 5

HCID 8028TetrahydrofuranHCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 53592776-ChloropurineHCID 539584884-Di(propan-2-yloxy)phosphorylbut-3-en-1-ol

Product 1

HCID 536803136-Chloro-9-[4-di(propan-2-yloxy)phosphorylbut-3-enyl]purine

Sources & evidence

ORD record
ord-b939bbbe627d4832aeaec072fd310a6e
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Linked notes

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