Isobutyryl chloride → HCID 21893492, compound

HRID 1358679Notes

Reaction equation

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

Participants

Reactant 2

HCID 62325Isobutyryl chloride

HCID 21893565HCID 21893565, compound

Product 1

HCID 21893492HCID 21893492, compound

Procedure

The title compound was prepared following the method of Example 147 and using 1 mL of a stock solution of 0.6 g (1.8 mmol) of material from Example 50 and0.11 μL (0.11 mmol) isobutyryl chloride. NMR was consistent with the proposed compound.

Sources & evidence

ORD record: ord-bd8bed94bc3d4e12b9c3e02edbcd0578
Source dataset: uspto-grants-2003_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06596716B2

Reaction notes

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