Isocyanic acid, p-methoxybenzyl- → HCID 44218105, compound

HRID 1931492Notes

Reaction equation

HRID 1931492 reaction equation
[C@H:1]1([NH:10][C:11]2[CH:20]=[CH:19][C:18]3[C:13](=[CH:14][CH:15]=[C:16]([NH2:21])[CH:17]=3)[N:12]=2)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.[CH3:22][O:23][C:24]1[CH:33]=[CH:32][C:27]([CH2:28][N:29]=[C:30]=[O:31])=[CH:26][CH:25]=1>>[C@H:1]1([NH:10][C:11]2[CH:20]=[CH:19][C:18]3[C:13](=[CH:14][CH:15]=[C:16]([NH:21][C:30]([NH:29][CH2:28][C:27]4[CH:32]=[CH:33][C:24]([O:23][CH3:22])=[CH:25][CH:26]=4)=[O:31])[CH:17]=3)[N:12]=2)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1

Participants

3

Procedure

The title compound, MS: m/e=439.7 (M+H+), was prepared in accordance with the general method 4 of example 16 from (R)—N2-indan-1-yl-quinoline-2,6-diamine and 4-methoxybenzyl isocyanate.

Sources & evidence

ORD record
ord-e01fa0e5e47441e9808454849884db58
Source dataset
uspto-grants-2012_05
Patent number
US08188284B2

Reaction notes

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