HCID 10571424, compound → HCID 11793793, compound

HRID 363308Notes

Reaction equation

HRID 363308 reaction equation
NC1C=C(C2SC3C=CC=CC=3N=2)C([O:8][S:9]([C:12]([F:15])([F:14])[F:13])(=[O:11])=[O:10])=CC=1.[N:25]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=1[C:34]1[S:35][C:36]2[CH:42]=[CH:41][CH:40]=[CH:39][C:37]=2[N:38]=1)=[N+]=[N-]>>[NH2:25][C:28]1[CH:33]=[CH:32][C:31]([O:11][S:9]([C:12]([F:15])([F:14])[F:13])(=[O:10])=[O:8])=[CH:30][C:29]=1[C:34]1[S:35][C:36]2[CH:42]=[CH:41][CH:40]=[CH:39][C:37]=2[N:38]=1

Participants

3

Reactant 2

HCID 10571424HCID 10571424, compoundHCID 123424152-(2-Azidophenyl)-1,3-benzothiazole

Product 1

HCID 11793793HCID 11793793, compound

Procedure

This compound was prepared in a similar way to the compound of Example XIV from 2-(2-azidophenyl)benzothiazole (Found: M+ 374. C14H9F3N2O3S2 requires MW 374).

Sources & evidence

ORD record
ord-3de9281ebd824b038b75ce1170d441a0
Source dataset
uspto-grants-1999_02
Patent number
US05874431

Reaction notes

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