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Dimethyl Sulfoxide → HCID 86651562, compound

HRID 124611
Notes
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Reaction equation

HRID 124611 reaction equation
[Br:18][CH2:19][CH:20]1[CH2:21][CH2:22]1.[C:23](=[O:24])([O-:25])[O-:26].[CH3:29][CH2:30][O:31][C:32]([CH3:33])=[O:34].[CH3:35][S:36]([CH3:37])=[O:38].[Cl:1][c:2]1[n:3][c:4]2[c:9]([cH:10][n:11]1)[NH:8][C:7](=[O:12])[C:6]1([CH3:17])[N:5]2[CH2:16][CH2:15][O:14][CH2:13]1.[K+:27].[K+:28].[OH2:39]>>[Cl:1][c:2]1[n:3][c:4]2[c:9]([cH:10][n:11]1)[N:8]([CH2:19][CH:20]1[CH2:21][CH2:22]1)[C:7](=[O:12])[C:6]1([CH3:17])[N:5]2[CH2:16][CH2:15][O:14][CH2:13]1
ParticipantsSources & evidenceReaction notes

Participants

8

Reactant 7

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 962WaterHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 81503BromomethylcyclopropaneHCID 781653422-chloro-6a-methyl-6a,7,9,10-tetrahydro-[1,4]oxazino[3,4-h]pteridin-6(5H)-one

Product 1

Sources & evidence

ORD record
ord-275cdc7187ed4f89a335907a7cc2ca37
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes
HCID 86651562
HCID 86651562, compound