Isobutyryl chloride → HCID 9817382, compound

HRID 1167230Notes

Reaction equation

HRID 1167230 reaction equation
[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[CH:11]=[CH:10][C:9]([CH:12]([CH3:15])[CH2:13][NH2:14])=[CH:8][CH:7]=2)=[CH:2]1.[C:16](Cl)(=[O:20])[CH:17]([CH3:19])[CH3:18]>>[S:1]1[CH:5]=[CH:4][C:3]([C:6]2[CH:11]=[CH:10][C:9]([CH:12]([CH3:15])[CH2:13][NH:14][C:16](=[O:20])[CH:17]([CH3:19])[CH3:18])=[CH:8][CH:7]=2)=[CH:2]1

Participants

3

Reactant 2

HCID 62325Isobutyryl chlorideHCID 10727517HCID 10727517, compound

Product 1

HCID 9817382HCID 9817382, compound

Procedure

The title compound was prepared from 2-(4-(3-thienyl)phenyl)propylamine (see example 14) and isobutyryl chloride in a manner analogous to the procedure described in example 14. The NMR spectrum was consistent with the proposed title structure.

Sources & evidence

ORD record
ord-1d30b4e3c71542a5a92f6218c73a2f12
Source dataset
uspto-grants-2003_09
Patent number
US06617351B1

Reaction notes

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