HCID 18471048, compound → HCID 54053632, compound

HRID 2228715Notes

Reaction equation

HRID 2228715 reaction equation
[SH:1][C:2]1[S:3][C:4]2[CH2:14][CH2:13][C:12]3[C:7](=[CH:8][CH:9]=[CH:10][C:11]=3[O:15][CH2:16][C:17]([O:19]CC)=[O:18])[C:5]=2[N:6]=1.[F:22][C:23]1[CH:24]=[C:25]([CH:29](Br)[C:30]2[CH:35]=[CH:34][CH:33]=[C:32]([F:36])[CH:31]=2)[CH:26]=[CH:27][CH:28]=1>>[F:22][C:23]1[CH:24]=[C:25]([CH:29]([C:30]2[CH:35]=[CH:34][CH:33]=[C:32]([F:36])[CH:31]=2)[S:1][C:2]2[S:3][C:4]3[CH2:14][CH2:13][C:12]4[C:7](=[CH:8][CH:9]=[CH:10][C:11]=4[O:15][CH2:16][C:17]([OH:19])=[O:18])[C:5]=3[N:6]=2)[CH:26]=[CH:27][CH:28]=1

Participants

3

Reactant 2

HCID 18471048HCID 18471048, compoundHCID 178472952Ethyl[(2-mercapto-4,5-dihydronaphtho[1,2-d]thiazol-6-yl)oxy)acetate

Product 1

HCID 54053632HCID 54053632, compoundYield 47%

Procedure

Using ethyl [(2-mercapto-4,5-dihydronaphto[1,2-d]thiazol-6-yl)oxy]acetate and bis (3-fluorophenyl)methylbromide, the procedure of Example 63 was otherwise repeated to synthesize the title compound. Yield 47%.

Sources & evidence

ORD record
ord-d23d06fe5dd3485ca7aba7a353fbd45c
Source dataset
uspto-grants-2002_07
Patent number
US06417213B2

Reaction notes

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