Tert-Butylamine → HCID 10341025, compound

HRID 1173325Notes

Reaction equation

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

Participants

Reactant 2

HCID 6385Tert-Butylamine

HCID 86636725HCID 86636725, compound

Product 1

HCID 10341025HCID 10341025, compound

Procedure

Using the procedure described in Step B of Example 8 above, the product of Step A and tert-butylamine were converted to the title compound.

Sources & evidence

ORD record: ord-f50fd0fd84dc4ea3a173b1fac745cdbb
Source dataset: uspto-grants-2010_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07834062B2

Reaction notes

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