4-Methoxy-1,3-dihydro-2-benzofuran-1,3-dione → HCID 53764367, compound

HRID 1084993Notes

Reaction equation

C(O)(=O)C.[CH3:5][O:6][P:7]([CH2:27][NH2:28])([CH2:9][CH:10]([C:15](=[O:26])[NH:16][C@H:17]([C:22](=[O:25])[NH:23][CH3:24])[CH2:18][CH:19]([CH3:21])[CH3:20])[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:8].[CH3:29][O:30][C:31]1[CH:41]=[CH:40][CH:39]=[C:33]2[C:34]([O:36][C:37](=O)[C:32]=12)=[O:35]>>[CH3:5][O:6][P:7]([CH2:27][N:28]1[C:37](=[O:36])[C:32]2=[C:31]([O:30][CH3:29])[CH:41]=[CH:40][CH:39]=[C:33]2[C:34]1=[O:35])([CH2:9][CH:10]([C:15](=[O:26])[NH:16][C@H:17]([C:22](=[O:25])[NH:23][CH3:24])[CH2:18][CH:19]([CH3:21])[CH3:20])[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:8]

Participants

Reactant 2

HCID 2911934-Methoxy-1,3-dihydro-2-benzofuran-1,3-dione

HCID 86743557(aminomethyl)[(RS)-4-methyl-2-[[(S)-3-methyl-1-(methylcarbamoyl)butyl]carbamoyl]pentyl]phosphinic acid methyl ester acetate

Product 1

HCID 53764367HCID 53764367, compoundYield 20.2%

Procedure

In a manner analogous to that described in Example 3 (A), from 0.4 g of (aminomethyl)[(RS)-4-methyl-2-[[(S)-3-methyl-1-(methylcarbamoyl)butyl]carbamoyl]pentyl]phosphinic acid methyl ester acetate and 0.178 g of 3-methoxy-phthalic anhydride, there was obtained 0.1 g of [(3-methoxyphthalimido)methyl][(RS)-4-methyl-2-[[(S)-3-methyl-1-(methylcarbamoyl)butyl]carbamoyl]pentyl]phosphinic acid methyl ester in the form of a colorless foam.

Sources & evidence

ORD record: ord-e7b67db4bd9f40deb209d2b124f118cc
Source dataset: uspto-grants-1991_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05006651

Reaction notes

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