Isobutyryl chloride → HCID 22993352, compound

HRID 1167619Notes

Reaction equation

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

Participants

Reactant 2

HCID 62325Isobutyryl chloride

HCID 22993358HCID 22993358, compound

Product 1

HCID 22993352HCID 22993352, compound

Procedure

The procedure is as in Example 15, starting from the compound obtained in Step A and with the replacement of benzoyl chloride with isobutyryl chloride.

Sources & evidence

ORD record: ord-2a4baf5d2fd643678fbbdca31ab63f8b
Source dataset: uspto-grants-2003_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06620809B2

Reaction notes

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