Ethyl hydantoate → HCID 10584233, compound

HRID 1416399Notes

Reaction equation

[C:1]([NH:4][CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])(=[O:3])[NH2:2].C([O:18][CH:19](O)[C:20](OCC1C=CC=CC=1)=[O:21])C1C=CC=CC=1.[N+](C1C=C(C=CC=1)CN1C(=O)C(=O)N(CC(O)=O)C1=C)([O-])=O>>[OH:21][CH:20]1[N:4]([CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])[C:1](=[O:3])[NH:2][C:19]1=[O:18]

Participants

Reactant 3

HCID 222535Ethyl hydantoate

HCID 10638264HCID 10638264, compound

HCID 10849786HCID 10849786, compound

Product 1

HCID 10584233HCID 10584233, compound

Procedure

Ethyl N-carbamoylaminoacetate was made to react with benzyl 2-benzyloxy-2-hydroxyacetate in the same manner as mentioned in Example 8 paragraph (1) to give ethyl 5-hydroxy-2,4-dioxoimidazolidine-1-acetate.

Sources & evidence

ORD record: ord-95ea9bd8b1514fa0a266a2801a4fb48b
Source dataset: uspto-grants-1999_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05912261

Reaction notes

Loading…