Potassium Cation → HCID 86651582, compound

HRID 290073Notes

Reaction equation

[C:30]([O:31][CH2:32][CH3:33])(=[O:34])[CH3:35].[CH3:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41].[Cl:1][c:2]1[n:3][c:4]2[c:9]([cH:10][n:11]1)[NH:8][C:7](=[O:12])[CH:6]1[N:5]2[CH2:16][CH2:15][O:14][CH2:13]1.[I:17][CH2:18][C:19](=[O:20])[O:21][CH2:22][CH3:23].[K+:24].[K+:25].[O-:26][C:27]([O-:28])=[O:29].[O:42]=[CH:43][N:44]([CH3:45])[CH3:46]>>[Cl:1][c:2]1[n:3][c:4]2[c:9]([cH:10][n:11]1)[N:8]([CH2:18][C:19](=[O:20])[O:21][CH2:22][CH3:23])[C:7](=[O:12])[CH:6]1[N:5]2[CH2:16][CH2:15][O:14][CH2:13]1

Participants

Reactant 7

HCID 813Potassium Cation2×

HCID 6228Dimethylformamide

HCID 8058Hexane

HCID 8857Ethyl Acetate

HCID 12183Ethyl iodoacetate

HCID 19660Carbonate Ion

HCID 866515602-chloro-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-6(5H)-one

Product 1

HCID 86651582HCID 86651582, compound

Sources & evidence

ORD record: ord-f0128671f47841d9a17f6b9506fb1920
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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