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2-Aminothiazole → HCID 10020953, compound

HRID 666854
Notes
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Reaction equation

HRID 666854 reaction equation
[Br:20][N:21]1[C:22](=[O:23])[CH2:24][CH2:25][C:26]1=[O:27].[CH2:53]([Cl:54])[Cl:55].[CH:28]([CH3:29])([CH3:30])[n:31]1[cH:32][c:33]([C:44](=[O:45])[OH:46])[c:34]2[cH:35][cH:36][c:37]([C:40]([F:41])([F:42])[F:43])[cH:38][c:39]12.[NH2:47][c:48]1[s:49][cH:50][cH:51][n:52]1.[c:1]1([P:2]([c:3]2[cH:4][cH:5][cH:6][cH:7][cH:8]2)[c:9]2[cH:10][cH:11][cH:12][cH:13][cH:14]2)[cH:15][cH:16][cH:17][cH:18][cH:19]1>>[CH:28]([CH3:29])([CH3:30])[n:31]1[cH:32][c:33]([C:44](=[O:46])[NH:47][c:48]2[s:49][cH:50][cH:51][n:52]2)[c:34]2[cH:35][cH:36][c:37]([C:40]([F:41])([F:42])[F:43])[cH:38][c:39]12
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 21552-AminothiazoleHCID 6344DichloromethaneHCID 11776TriphenylphosphineHCID 67184N-bromobutanimideHCID 22497225HCID 22497225, compound

Product 1

HCID 10020953HCID 10020953, compound

Sources & evidence

ORD record
ord-848335c22bda48d79fdd85aece998305
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes