HCID 13473381, compound → HCID 140352895, compound

HRID 1195057Notes

Reaction equation

HRID 1195057 reaction equation
[NH2:1][C@H:2]1[C@@H:5]([CH2:6][O:7][C:8](=[O:10])[NH2:9])[N:4]([S:11]([OH:14])(=[O:13])=[O:12])[C:3]1=[O:15].[NH2:16][C:17]1[S:18][CH:19]=[C:20](/[C:22](=[N:26]/[O:27][CH2:28][CH2:29][N:30]=[N+:31]=[N-:32])/[C:23](O)=[O:24])[N:21]=1>>[NH2:16][C:17]1[S:18][CH:19]=[C:20](/[C:22](=[N:26]/[O:27][CH2:28][CH2:29][N:30]=[N+:31]=[N-:32])/[C:23]([NH:1][C@H:2]2[C@@H:5]([CH2:6][O:7][C:8](=[O:10])[NH2:9])[N:4]([S:11]([OH:14])(=[O:12])=[O:13])[C:3]2=[O:15])=[O:24])[N:21]=1

Participants

3

Reactant 2

HCID 13473381HCID 13473381, compoundHCID 21269061HCID 21269061, compound

Product 1

HCID 140352895HCID 140352895, compoundYield 59%

Procedure

In the same manner as described in Example 9, from 1.87 g of (3S,4S)-3-amino-4-carbamoyloxymethyl-2-oxo-1-azetidinesulphonic acid and 2 g of 2-(2-amino-4-thiazolyl)-2-[(Z)-(2-azidoethoxy)imino]-acetic acid there are obtained 2.2 g of (3S,4S)-3-[(Z)-2-(2-amino-4-thiazolyl)-2-[(2-azidoethoxy)imino]acetamido]-4-carbamoyloxymethyl-2-oxo-1-azetidinesulphonic acid.

Sources & evidence

ORD record
ord-03251b7d5a56454fbf019cbc374bdf83
Source dataset
uspto-grants-1989_03
Patent number
US04816582

Reaction notes

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