Isopropyl isocyanate → HCID 44223218, compound

HRID 1803082Notes

Reaction equation

HRID 1803082 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([N+:12]([O-])=O)[CH:8]=2)[N:3]=1.[CH3:15][C:16]1[O:20][C:19]([CH2:21][NH2:22])=[CH:18][CH:17]=1.[CH:23]([N:26]=[C:27]=[O:28])([CH3:25])[CH3:24]>>[CH:23]([NH:26][C:27]([NH:12][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:22][CH2:21][C:19]1[O:20][C:16]([CH3:15])=[CH:17][CH:18]=1)[CH:11]=[CH:10]2)=[O:28])([CH3:25])[CH3:24]

Participants

4

Reactant 3

HCID 61277Isopropyl isocyanateHCID 27246835-Methyl-2-furylmethylamineHCID 109217232-Chloro-6-nitroquinoline

Product 1

HCID 44223218HCID 44223218, compound

Procedure

The title compound, MS: m/e=339.3 (M+H+), was prepared in accordance with the general method of example 14 from 2-chloro-6-nitro-quinoline, 5-methyl-2-furanmethanamine and isopropyl isocyanate.

Sources & evidence

ORD record
ord-cdad36f197eb431ca44f0307428ecae9
Source dataset
uspto-grants-2013_01
Patent number
US08350028B2

Reaction notes

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