HCID 68284413, compound → HCID 86673810, compound

HRID 1527188Notes

Reaction equation

HRID 1527188 reaction equation
[C:1]([O:5][C:6](=[O:17])[CH2:7]C1C=C2C(C=CN2)=CC=1)([CH3:4])([CH3:3])[CH3:2].C(O[C:22]1[CH:23]=[C:24]2[C:28](=[CH:29][CH:30]=1)[N:27]([C:31]([NH2:33])=[O:32])[CH:26]=[C:25]2[N:34]=[C:35]=[O:36])C=C>>[C:1]([O:5][C:6](=[O:17])[CH2:7][C:30]1[CH:29]=[C:28]2[C:24]([C:25]([N:34]=[C:35]=[O:36])=[CH:26][N:27]2[C:31](=[O:32])[NH2:33])=[CH:23][CH:22]=1)([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 68284413HCID 68284413, compoundHCID 866737945-Allyloxy-3-isocyanato-indole-1-carboxylic acid amide

Product 1

HCID 86673810HCID 86673810, compound

Procedure

was prepared from (1H-indol-6-yl)-acetic acid tert-butyl 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-2d8b05de336347cb8993226682e335f6
Source dataset
uspto-grants-2015_07
Patent number
US09085555B2

Reaction notes

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