Methoxyacetyl chloride → HCID 18368073, compound

HRID 379789Notes

Reaction equation

HRID 379789 reaction equation
[NH2:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[CH:9]=2)[N:4]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[C:3]=1[C:19](=[O:27])[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH3:26])[CH:21]=1.[CH3:28][O:29][CH2:30][C:31](Cl)=[O:32]>>[CH2:17]([O:16][C:14]([N:4]1[C:5]2[C:10](=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][CH:6]=2)[C:2]([NH:1][C:31](=[O:32])[CH2:30][O:29][CH3:28])=[C:3]1[C:19](=[O:27])[C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH3:26])[CH:21]=1)=[O:15])[CH3:18]

Participants

3

Reactant 2

HCID 96623Methoxyacetyl chlorideHCID 183682013-Amino-1-(ethoxycarbonyl)-2-(3-methylbenzoyl)-5-nitroindole

Product 1

HCID 18368073HCID 18368073, compound

Procedure

The title compound was prepared according to the procedure described in step 1 of Example 2 (Method A) from 3-amino-2-(3-chlorobenzoyl)-1-(ethoxycarbonyl)-5-nitroindole (step 1) and methoxyacetyl chloride.

Sources & evidence

ORD record
ord-6efd80caab4341b18735d8eafe4916ef
Source dataset
uspto-grants-2001_10
Patent number
US06300363B1

Reaction notes

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