Neopentylamine → HCID 11548673, compound

HRID 1723959Notes

Reaction equation

[C:1]([C:5]1[CH:6]=[C:7]([NH:31][S:32]([CH3:35])(=[O:34])=[O:33])[C:8]([O:29][CH3:30])=[C:9]([NH:11][C:12]([C:14]2[CH:15]=[CH:16][C:17]([CH3:28])=[C:18]([N:20]3[CH:24]=[C:23]([C:25](O)=[O:26])[N:22]=[CH:21]3)[CH:19]=2)=[O:13])[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:36]([NH2:41])[C:37]([CH3:40])([CH3:39])[CH3:38]>>[CH3:38][C:37]([CH3:40])([CH3:39])[CH2:36][NH:41][C:25]([C:23]1[N:22]=[CH:21][N:20]([C:18]2[CH:19]=[C:14]([C:12](=[O:13])[NH:11][C:9]3[CH:10]=[C:5]([C:1]([CH3:3])([CH3:4])[CH3:2])[CH:6]=[C:7]([NH:31][S:32]([CH3:35])(=[O:34])=[O:33])[C:8]=3[O:29][CH3:30])[CH:15]=[CH:16][C:17]=2[CH3:28])[CH:24]=1)=[O:26]

Participants

Reactant 2

HCID 79882Neopentylamine

HCID 57559701HCID 57559701, compound

Product 1

HCID 11548673HCID 11548673, compound

Procedure

The above carboxylic acid was then coupled with neopentylamine using the coupling procedure described in Example 4 to provide the title compound. 134-136° C.; ESI MS m/z 570 [C29H39N5O5S +H]+.

Sources & evidence

ORD record: ord-2dfc2396542f4dab9c6b3fde8887f861
Source dataset: uspto-grants-2009_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07485657B2

Reaction notes

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