HCID 13496813, compound → HCID 18368181, compound

HRID 379862Notes

Reaction equation

HRID 379862 reaction equation
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([Cl:11])=[CH:8][CH:9]=2)[NH:4][C:3]=1[C:12](=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[CH2:20]([O:27][CH:28]([CH3:33])[CH2:29][C:30](Cl)=[O:31])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[C:12]([C:3]1[NH:4][C:5]2[C:10]([C:2]=1[NH:1][C:30](=[O:31])[CH2:29][CH:28]([O:27][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH3:33])=[CH:9][CH:8]=[C:7]([Cl:11])[CH:6]=2)(=[O:19])[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

3

Reactant 2

HCID 13496813HCID 13496813, compoundHCID 183679723-Amino-2-benzoyl-6-chloroindole

Product 1

HCID 18368181HCID 18368181, compound

Procedure

The titled compound was prepared according to the procedure described in Example 19 employing 3-amino-2-benzoyl-6-chloroindole (Example 1) and 3-benzyloxybutyryl chloride (Eberlein, T. H. et al., J. Org. Chem. 1992, 57, 3479).

Sources & evidence

ORD record
ord-1bc8aed1f4da4d63afe268052ec33725
Source dataset
uspto-grants-2001_10
Patent number
US06300363B1

Reaction notes

Loading…