Diisopropylamine → HCID 11624326, compound

HRID 1224311Notes

Reaction equation

HRID 1224311 reaction equation
[CH2:46]1[CH2:49][CH2:48][CH2:47][O:50]1.[CH3:2][CH:3]([N-:4][CH:5]([CH3:6])[CH3:7])[CH3:8].[CH3:9][CH2:10][CH2:11][CH2:12][Li:13].[CH:14]([NH:15][CH:16]([CH3:17])[CH3:18])([CH3:19])[CH3:20].[Li+:1].[NH:21]([c:22]1[cH:23][cH:24][cH:25][cH:26][cH:27]1)[c:28]1[n:29](-[c:40]2[cH:41][cH:42][cH:43][cH:44][cH:45]2)[c:30]2[n:31][cH:32][cH:33][c:34]([CH3:39])[c:35]2[c:36](=[O:38])[cH:37]1>>[NH:21]([c:22]1[cH:23][cH:24][cH:25][cH:26][cH:27]1)[c:28]1[n:29](-[c:40]2[cH:41][cH:42][cH:43][cH:44][cH:45]2)[c:30]2[n:31][cH:32][cH:33][c:34]([CH2:39][OH:50])[c:35]2[c:36](=[O:38])[cH:37]1

Participants

7

Reactant 6

HCID 7912DiisopropylamineHCID 8028TetrahydrofuranHCID 28486Lithium ionHCID 5062348DiisopropylamideHCID 10131414HCID 10131414, compoundHCID 178418339Butyllithium

Product 1

HCID 11624326HCID 11624326, compound

Sources & evidence

ORD record
ord-1da0851220e842f897c03f92da68cbc6
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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