Isopropyl isocyanate → HCID 44223273, compound

HRID 1803080Notes

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][O:16][C:17]1[CH:24]=[CH:23][C:20]([CH2:21][NH2:22])=[CH:19][CH:18]=1.[CH:25]([N:28]=[C:29]=[O:30])([CH3:27])[CH3:26]>>[CH:25]([NH:28][C:29]([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:20]1[CH:23]=[CH:24][C:17]([O:16][CH3:15])=[CH:18][CH:19]=1)[CH:11]=[CH:10]2)=[O:30])([CH3:27])[CH3:26]

Participants

Reactant 3

HCID 61277Isopropyl isocyanate

HCID 754524-Methoxybenzylamine

HCID 109217232-Chloro-6-nitroquinoline

Product 1

HCID 44223273HCID 44223273, compound

Procedure

The title compound, MS: m/e=365.1 (M+H+), was prepared in accordance with the general method of example 14 from 2-chloro-6-nitro-quinoline, 4-methoxy-benzylamine and isopropyl isocyanate.

Sources & evidence

ORD record: ord-541d41c7bea748ce9736bed1fe616020
Source dataset: uspto-grants-2013_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08350028B2

Reaction notes

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