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6-Chloro-2-benzothiazolamine → 2-Amino-6-fluorobenzothiazole

HRID 223387
Notes
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Reaction equation

HRID 223387 reaction equation
ClCl.BrBr.N([O-])=O.[Na+].ClC1SC2C=C(Cl)C=CC=2N=1.Cl[C:21]1[CH:30]=[CH:29][C:24]2[N:25]=[C:26]([NH2:28])[S:27][C:23]=2[CH:22]=1.ClC1SC2C=C([F:41])C=CC=2N=1>>[F:41][C:21]1[CH:30]=[CH:29][C:24]2[N:25]=[C:26]([NH2:28])[S:27][C:23]=2[CH:22]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 72266-Chloro-2-benzothiazolamineHCID 24408BromineHCID 24526ChlorineHCID 771762,6-DichlorobenzothiazoleHCID 20498702-Chloro-6-fluorobenzothiazoleHCID 23668193Sodium Nitrite

Product 1

HCID 319954
2-Amino-6-fluorobenzothiazole

Procedure

The starting compounds of the formula III wherein X is chlorine or bromine can be prepared from corresponding 2-benzothiazole-amines by reaction with a warm concentrated hydrohalic acid and sodium nitrite [See H. Mazzone and G. Pappalardo, Il Farmaco, Ed. Sc. 32, 348-354 (1977)]. Thus, for example, 2,6-dichlorobenzothiazole (m.p. 99°-101° C.) can be obtained from 6-chloro-2-benzothiazole-amine, and 2-chloro-6-fluorobenzothiazole (m.p. 92°-93° C.) can be obtained from 6-fluoro-2-benzothiazole-amine.

Sources & evidence

ORD record
ord-b453363a4d5f450080ec690120e5aa05
Source dataset
uspto-grants-1982_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04353919

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes