Benzylamine → HCID 21103282, compound

HRID 1354077Notes

Reaction equation

C(O[C:4]([CH2:6][N:7]([S:15]([C:18]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=1)(=[O:17])=[O:16])[CH:8]([CH2:13]O)[C:9]([O:11][CH3:12])=[O:10])=[O:5])C.[CH2:26]([NH2:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[CH2:26]([N:33]1[C:4](=[O:5])[CH2:6][N:7]([S:15]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)(=[O:17])=[O:16])[CH:8]([C:9]([O:11][CH3:12])=[O:10])[CH2:13]1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

Participants

Reactant 2

HCID 7504Benzylamine

HCID 11234214HCID 11234214, compound

Product 1

HCID 21103282HCID 21103282, compound

Procedure

A title compound was prepared by the same method as in Example 4, except that the compound of Example 3 and benzylamine were used.

Sources & evidence

ORD record: ord-d1f2cfce29b744b498603496d2afffcd
Source dataset: uspto-grants-2007_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07223751B2

Reaction notes

Loading…