Benzoyl chloride, 3,4,5-trimethoxy- → HCID 20226427, compound

HRID 1732030Notes

Reaction equation

HRID 1732030 reaction equation
[NH2:1][CH:2]1[CH2:6][N:5]([CH3:7])[N:4]([CH3:8])[CH2:3]1.[CH3:9][O:10][C:11]1[CH:12]=[C:13]([CH:17]=[C:18]([O:22][CH3:23])[C:19]=1[O:20][CH3:21])[C:14](Cl)=[O:15]>>[CH3:23][O:22][C:18]1[CH:17]=[C:13]([CH:12]=[C:11]([O:10][CH3:9])[C:19]=1[O:20][CH3:21])[C:14]([NH:1][CH:2]1[CH2:6][N:5]([CH3:7])[N:4]([CH3:8])[CH2:3]1)=[O:15]

Participants

3

Reactant 2

HCID 78282Benzoyl chloride, 3,4,5-trimethoxy-HCID 20226460HCID 20226460, compound

Product 1

HCID 20226427HCID 20226427, compound

Procedure

The title compound was prepared as described in Example 3 of U.S. Pat. No. 4,207,327 from 4-amino-1,2-dimethylpyrazolidine and 3,4,5-trimethoxybenzoyl chloride, m.p. 163°-166° C.

Sources & evidence

ORD record
ord-a4b37405f92740b7b2efebb1e83f2a2e
Source dataset
uspto-grants-1986_11
Patent number
US04624961

Reaction notes

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