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Diisopropylamine → HCID 12067664, compound

HRID 202874
Notes
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Reaction equation

HRID 202874 reaction equation
[CH2:8]([Li:9])[CH2:10][CH2:11][CH3:12].[CH3:13][O:14][C:15]([CH2:16][c:17]1[cH:18][c:19]([Br:25])[c:20]([S:23][CH3:24])[cH:21][cH:22]1)=[O:26].[CH3:39][N:40]1[CH2:41][CH2:42][CH2:43][N:44]([CH3:45])[C:46]1=[O:47].[CH:1]([NH:2][CH:3]([CH3:4])[CH3:5])([CH3:6])[CH3:7].[I:27][CH2:28][CH:29]1[CH2:30][CH2:31][CH2:32][CH2:33]1.[O:34]1[CH2:35][CH2:36][CH2:37][CH2:38]1>>[CH3:13][O:14][C:15]([CH:16]([c:17]1[cH:18][c:19]([Br:25])[c:20]([S:23][CH3:24])[cH:21][cH:22]1)[CH2:28][CH:29]1[CH2:30][CH2:31][CH2:32][CH2:33]1)=[O:26]
ParticipantsSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 7912DiisopropylamineHCID 8028TetrahydrofuranHCID 816462(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 2762531(Iodomethyl)cyclopentaneHCID 12067663(3-Bromo-4-methylsulfanyl-phenyl)-acetic acid methyl esterHCID 178418339Butyllithium

Product 1

HCID 12067664
HCID 12067664, compound

Sources & evidence

ORD record
ord-0383150cd02e4571a14b6d8752d51617
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes