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Hydrogen Sulfide → HCID 23370042, compound

HRID 87099
Notes
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Reaction equation

HRID 87099 reaction equation
[C:1](#[N:2])[c:3]1[cH:4][cH:5][c:6]([C:9](=[O:10])[NH:11][C:12]([NH:13][c:14]2[cH:15][cH:16][c:17]([O:18][CH2:19][C:20](=[O:21])[O:22][C:23]([CH3:24])([CH3:25])[CH3:26])[cH:27][cH:28]2)=[O:29])[cH:7][n:8]1.[CH3:37][CH2:38][N:39]([CH2:40][CH3:41])[CH2:42][CH3:43].[SH2:36].[cH:30]1[cH:31][cH:32][n:33][cH:34][cH:35]1>>[C:1]([NH2:2])([c:3]1[cH:4][cH:5][c:6]([C:9](=[O:10])[NH:11][C:12]([NH:13][c:14]2[cH:15][cH:16][c:17]([O:18][CH2:19][C:20](=[O:21])[O:22][C:23]([CH3:24])([CH3:25])[CH3:26])[cH:27][cH:28]2)=[O:29])[cH:7][n:8]1)=[S:36]
ParticipantsSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 402Hydrogen SulfideHCID 1049PyridineHCID 8471TriethylamineHCID 23369993t-Butyl 4-[3-(6-cyanopyrid-3-ylcarbonyl)ureido]phenoxyacetate

Product 1

HCID 23370042HCID 23370042, compound

Sources & evidence

ORD record
ord-24169a8573f14988bcc5d4784ee77252
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