HCID 53716008, compound → HCID 54040437, compound

HRID 1463441Notes

Reaction equation

HRID 1463441 reaction equation
N[C@@H]1[C:8](=[O:9])[N:7]2[C@@H]1S[C@](C(O)=O)(N1CCN(N=CC3C=CC(C)=CC=3)C1=O)C2.[NH2:28][C@@H:29]1[C:35](=[O:36])[N:34]2[C@@H:30]1[S:31][C@@:32]([N:40]1[CH2:44][CH2:43][N:42]([N:45]=CC3C=CC=C(OC)C=3)[C:41]1=[O:55])([C:37]([OH:39])=[O:38])[CH2:33]2>>[NH2:28][C@@H:29]1[C:35](=[O:36])[N:34]2[C@@H:30]1[S:31][C@:32]([C:37]([OH:39])=[O:38])([N:40]1[CH2:44][CH2:43][N:42]([NH:45][C:8]([NH2:7])=[O:9])[C:41]1=[O:55])[CH2:33]2

Participants

3

Reactant 2

HCID 53716008HCID 53716008, compoundHCID 67830652HCID 67830652, compound

Product 1

HCID 54040437HCID 54040437, compound

Procedure

(3R,5R,6R)-6-amino-3-carboxy-3-(3-p-methylbenzylideneamino-2-oxoimidazolidin-1-yl)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane and (3R,5R,6R)-6-amino-3-(3-anisylideneamino-2-oxoimidazolidin-1-yl)-3-carboxy-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane were treated in the same manner to obtain (3R,5R,6R)-6-amino-3-carboxy-7-oxo-3-(2-oxo-3-ureidoimidazolidin-1-yl)-4-thia-1-azabicyclo[3.2.0]heptane. The physical property (IR) of this product were identical with that obtained above.

Sources & evidence

ORD record
ord-177288080fb240eea32fcd5f621db577
Source dataset
uspto-grants-1994_04
Patent number
US05300497

Reaction notes

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