3-Isocyanatobenzonitrile → HCID 131731508, compound

HRID 403880Notes

Reaction equation

HRID 403880 reaction equation
F[C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:35])[NH:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:18]=[C:19]4[C:23](=[CH:24][CH:25]=3)[C:22](=[O:26])[N:21]([C@@H:27]([CH:32]([CH3:34])[CH3:33])[C:28]([O:30][CH3:31])=[O:29])[CH2:20]4)=[CH:13][CH:12]=2)=[CH:4][CH:3]=1.[NH2:36][C:37]1C=CC(C2C=C3C(=CC=2)C(=O)N([C@@H](C(C)C)C(OC)=O)C3)=CC=1.C(C1C=C(N=C=O)C=CC=1)#N>>[C:37]([C:7]1[CH:6]=[C:5]([NH:8][C:9](=[O:35])[NH:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:18]=[C:19]4[C:23](=[CH:24][CH:25]=3)[C:22](=[O:26])[N:21]([C@@H:27]([CH:32]([CH3:33])[CH3:34])[C:28]([O:30][CH3:31])=[O:29])[CH2:20]4)=[CH:13][CH:12]=2)[CH:4]=[CH:3][CH:2]=1)#[N:36]

Participants

4

Reactant 3

HCID 27333153-IsocyanatobenzonitrileHCID 123620640(S)-Methyl 2-(5-(4-(3-(4-fluorophenyl)ureido)phenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoateHCID 131731499(S)-Methyl 2-(5-(4-aminophenyl)-1-oxoisoindolin-2-yl)-3-methylbutanoate

Product 1

HCID 131731508HCID 131731508, compound

Procedure

The compound of example 254 was prepared analogous to compound of example 224 by reaction of compound of example 223 with 3-cyanophenyl isocyanate. The compound of example 254 was used directly without isolation for the preparation of compound of example 255.

Sources & evidence

ORD record
ord-16c65e15597b41508d5f389b3aa84eeb
Source dataset
uspto-grants-2014_06
Patent number
US08748426B2

Reaction notes

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