Diisopropylamine → HCID 67483527, compound

HRID 700445Notes

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][cH:19][c:20]([N:23]2[CH2:24][CH2:25][O:26][CH2:27][CH2:28]2)[cH:21][cH:22]1)=[O:29].[CH3:42][N:43]1[CH2:44][CH2:45][CH2:46][N:47]([CH3:48])[C:49]1=[O:50].[CH:1]([NH:2][CH:3]([CH3:4])[CH3:5])([CH3:6])[CH3:7].[I:30][CH2:31][CH:32]1[CH2:33][CH2:34][CH2:35][CH2:36]1.[O:37]1[CH2:38][CH2:39][CH2:40][CH2:41]1>>[CH3:13][O:14][C:15]([CH:16]([c:17]1[cH:18][cH:19][c:20]([N:23]2[CH2:24][CH2:25][O:26][CH2:27][CH2:28]2)[cH:21][cH:22]1)[CH2:31][CH:32]1[CH2:33][CH2:34][CH2:35][CH2:36]1)=[O:29]

Participants

Reactant 6

HCID 7912Diisopropylamine

HCID 8028Tetrahydrofuran

HCID 816462(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-

HCID 2762531(Iodomethyl)cyclopentane

HCID 13703753(4-Morpholin-4-yl-phenyl)-acetic acid methyl ester

HCID 178418339Butyllithium

Product 1

HCID 67483527HCID 67483527, compound

Sources & evidence

ORD record: ord-9d83b6eaa35c410a93ff0a28f6e7617d
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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