1-Isocyanato-4-methoxybenzene → HCID 18663209, compound

HRID 1956362Notes

Reaction equation

HRID 1956362 reaction equation
[F:1][C:2]1[CH:30]=[CH:29][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][N:17]4[CH2:21][CH2:20][N:19]([C:22]5[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=5)[C:18]4=[O:28])[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1.[CH3:31][O:32]C1C=CC(N=C=O)=CC=1>>[F:1][C:2]1[CH:30]=[CH:29][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][N:17]4[CH2:21][CH2:20][N:19]([C:22]5[CH:27]=[CH:26][C:25]([O:32][CH3:31])=[CH:24][CH:23]=5)[C:18]4=[O:28])[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1

Participants

3

Reactant 2

HCID 794431-Isocyanato-4-methoxybenzeneHCID 99532691-(2-(4-(6-FLUORO-1,2-BENZISOXAZOL-3-YL)-1-PIPERIDINYL)ETHYL)-3-PHENYL-2-IMIDAZOLIDINONE

Product 1

HCID 18663209HCID 18663209, compound

Procedure

This product is obtained in the same manner as the compound of Example 5, but with replacement of the phenyl isocyanate by 4-methoxyphenyl isocyanate in Step 1 of the synthesis. The expected product melts at 154°-157° C.

Sources & evidence

ORD record
ord-ab5f5a6ffc1343efbdad7dcb47da1a69
Source dataset
uspto-grants-1998_07
Patent number
US05780474

Reaction notes

Loading…