HCID 54017257, compound → HCID 86673809, compound

HRID 1527185Notes

Reaction equation

HRID 1527185 reaction equation
[CH2:1]([O:3][C:4](=[O:15])[CH2:5]C1C=C2C(C=CN2)=CC=1)[CH3:2].C(O[C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[N:25]([C:29]([NH2:31])=[O:30])[CH:24]=[C:23]2[N:32]=[C:33]=[O:34])C=C>>[CH2:1]([O:3][C:4](=[O:15])[CH2:5][C:28]1[CH:27]=[C:26]2[C:22]([C:23]([N:32]=[C:33]=[O:34])=[CH:24][N:25]2[C:29](=[O:30])[NH2:31])=[CH:21][CH:20]=1)[CH3:2]

Participants

3

Reactant 2

HCID 54017257HCID 54017257, compoundHCID 866737945-Allyloxy-3-isocyanato-indole-1-carboxylic acid amide

Product 1

HCID 86673809HCID 86673809, compound

Procedure

was prepared from (1H-indol-6-yl)-acetic acid ethyl ester using the protocol described for steps B-E in scheme A4 for the preparation of 5-allyloxy-3-isocyanato-indole-1-carboxylic acid amide.

Sources & evidence

ORD record
ord-392a4b6fa7ac4bb692b473f8ba15a94d
Source dataset
uspto-grants-2015_07
Patent number
US09085555B2

Reaction notes

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