2-Chlorobenzothiazole → HCID 28832784, compound

HRID 1593520Notes

Reaction equation

Cl[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[F:11][C:12]([F:22])([F:21])[O:13][C:14]1[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=1>>[S:3]1[C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=[C:2]1[NH:18][C:17]1[CH:19]=[CH:20][C:14]([O:13][C:12]([F:11])([F:21])[F:22])=[CH:15][CH:16]=1

Participants

Reactant 2

HCID 119872-Chlorobenzothiazole

HCID 6008484-(Trifluoromethoxy)aniline

Product 1

HCID 28832784HCID 28832784, compound

Procedure

The title compound was synthesised from 2-chloro-benzothiazole (commercially available) and 4-trifluoromethoxyaniline (commercially available) according to the procedure described for Example A. MS (m/z): 310.0 (MH+, 100%).

Sources & evidence

ORD record: ord-036f60d9a77e424da984934f41e70aec
Source dataset: uspto-grants-2007_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07297707B2

Reaction notes

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