Isopropylamine → HCID 68123158, compound

HRID 972731Notes

Reaction equation

Cl[CH:2]([CH3:27])[C:3]([NH:5][C:6]1[C:22]([O:23][CH3:24])=[C:21]([O:25][CH3:26])[CH:20]=[CH:19][C:7]=1[CH2:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][N:10]=1)=[O:4].[CH:28]([NH2:31])([CH3:30])[CH3:29]>>[CH:28]([NH:31][CH:2]([CH3:27])[C:3]([NH:5][C:6]1[C:22]([O:23][CH3:24])=[C:21]([O:25][CH3:26])[CH:20]=[CH:19][C:7]=1[CH2:8][C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]=[CH:11][N:10]=1)=[O:4])([CH3:30])[CH3:29]

Participants

Reactant 2

HCID 6363Isopropylamine

HCID 12369646HCID 12369646, compound

Product 1

HCID 68123158HCID 68123158, compound

Procedure

Following the procedure of Example 1, but reacting 1-(2-[2-chloro-propionyl] amino-3,4-dimethoxybenzyl) isoquinoline with isopropylamine, there is obtained 1-(2[2-isopropylamino-propionyl] amino-3,4-dimethoxybenzyl) isoquinoline.

Sources & evidence

ORD record: ord-220a400f433647f88543f78831a3f72d
Source dataset: uspto-grants-1977_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04053603

Reaction notes

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