Pivaloyl chloride → HCID 57884006, compound

HRID 1817882Notes

Reaction equation

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

Participants

Reactant 2

HCID 62493Pivaloyl chloride

HCID 68874120HCID 68874120, compound

Product 1

HCID 57884006HCID 57884006, compound

Procedure

The title compound was prepared according to the procedure described in Step C of Example 17 from 4-(isopropylsulfonyl)-N′-(tetrahydro-2H-pyran-4-ylmethyl)benzene-1,2-diamine (Step B) and pivaloyl chloride.

Sources & evidence

ORD record: ord-31c4d8ffd41a4ce3868d2b45dd7d2877
Source dataset: uspto-grants-2009_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07598393B2

Reaction notes

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