HCID 18367786, compound → HCID 18368153, compound

HRID 379899Notes

Reaction equation

HRID 379899 reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([NH:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:3]=1.[C:16]([O:19][CH2:20][C:21]1[CH:25]=[CH:24][O:23][C:22]=1[C:26](=[O:29])[CH2:27]Br)(=[O:18])[CH3:17]>>[C:16]([O:19][CH2:20][C:21]1[CH:25]=[CH:24][O:23][C:22]=1[C:26]([C:27]1[N:10]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:4]2[C:5]([C:6]=1[NH2:7])=[CH:8][CH:9]=[C:2]([Cl:1])[CH:3]=2)=[O:29])(=[O:18])[CH3:17]

Participants

3

Reactant 2

HCID 18367786HCID 18367786, compoundHCID 183678884-Chloro-2-[(ethoxycarbonyl)amino]benzonitrile

Product 1

HCID 18368153HCID 18368153, compound

Procedure

The title compound was prepared according to the procedure described in Step 2 of Example 1 from 4-chloro-2-(ethoxycarbonylamino)benzonitrile (Example 1, step 1) and 3-acetoxymethyl-2-(bromoacetyl)furan (Example 372, step 1).

Sources & evidence

ORD record
ord-4135acce92e4429fb423f9f78507daba
Source dataset
uspto-grants-2001_10
Patent number
US06300363B1

Reaction notes

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