HCID 131710464, compound → HCID 131710462, compound

HRID 1287209Notes

Reaction equation

HRID 1287209 reaction equation
[Na].[S:2]([CH:6]([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:7]([NH:9][CH:10]1[C:27](=[O:28])[N:12]2[CH:13]=[C:14]([CH2:17][N+:18]3[CH:23]=[CH:22][C:21]([C:24]([O-:26])=[O:25])=[CH:20][CH:19]=3)[CH2:15][S:16][C@H:11]12)=[O:8])([OH:5])(=[O:4])=[O:3]>O>[S:2]([CH:6]([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[C:7]([NH:9][CH:10]1[C:27](=[O:28])[N:12]2[CH:13]=[C:14]([CH2:17][N+:18]3[CH:23]=[CH:22][C:21]([C:24]([O-:26])=[O:25])=[CH:20][CH:19]=3)[CH2:15][S:16][C@H:11]12)=[O:8])([OH:5])(=[O:4])=[O:3]

Participants

3

Procedure

In 10 ml. of distilled water is dissolved 1.0 g. of N-[7-(α-sulfophenylacetamido)ceph-3-em-3-ylmethyl]-pyridinium-4-carboxylate sodium salt and the solution is passed over an ion exchange resin (Amberlite IR-120 of Rohm and Haas Co., U.S.A.) to obtain an aqueous solution of free acid N-[7-(α-sulfophenylacetamido)-ceph-3-em-3-ylmethyl]pyridinium-4-carboxylate.

Sources & evidence

ORD record
ord-f8866cdca3414db5975929dbd127472b
Source dataset
uspto-grants-1976_10
Patent number
US03984403

Reaction notes

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