Sodium Iodide → HCID 131717060, compound

HRID 346394Notes

Reaction equation

HRID 346394 reaction equation
Cl[CH2:2][C:3]1[CH2:4][S:5][C@@H:6]2[C@H:26]([NH:27][C:28](=[O:58])[C:29](=[N:55][O:56][CH3:57])[C:30]3[N:31]=[C:32]([NH:35]C(C4C=CC=CC=4)(C4C=CC=CC=4)C4C=CC=CC=4)[S:33][CH:34]=3)[C:25](=[O:59])[N:7]2[C:8]=1[C:9]([O:11]C(C1C=CC=CC=1)C1C=CC=CC=1)=[O:10].[I-].[Na+:61].[SH:62][C:63]1[O:64][C:65]([C:68]2[CH:73]=[CH:72][CH:71]=[CH:70][CH:69]=2)=[CH:66][N:67]=1>>[NH2:35][C:32]1[S:33][CH:34]=[C:30]([C:29](=[N:55][O:56][CH3:57])[C:28]([NH:27][C@@H:26]2[C:25](=[O:59])[N:7]3[C:8]([C:9]([O-:11])=[O:10])=[C:3]([CH2:2][S:62][C:63]4[O:64][C:65]([C:68]5[CH:73]=[CH:72][CH:71]=[CH:70][CH:69]=5)=[CH:66][N:67]=4)[CH2:4][S:5][C@H:6]23)=[O:58])[N:31]=1.[Na+:61]

Participants

4

Procedure

The same operation as in EXAMPLE 65 was conducted by using 600 mg (0.71 mmol) of benzhydryl 3-chloromethyl-7β-[2-methoxyimino-2-( 2-tritylaminothiazol-4-yl)acetamido]-3-cephem-4-carboxylate (syn-isomer), 160 mg (1.07 mmol) of sodium iodide and 130 mg (0.72 mmol) of 2-mercapto-5-phenyloxazole, whereby 70 mg (yield: 7.1%) of the above identified compound was obtained.

Workup

  1. customwas obtained

Sources & evidence

ORD record
ord-13e35c5f3a68424cb9f11a63e0190ecd
Source dataset
uspto-grants-1991_10
Patent number
US05061794

Reaction notes

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