HCID 20368090, compound → HCID 20368120, compound

HRID 1283316Notes

Reaction equation

HRID 1283316 reaction equation
C[C:2]1[C:10]2[S:9][C:8]3=[N:11][CH:12]=[N:13][N:7]3[C:6]=2[CH:5]=[CH:4][CH:3]=1.F[C:15]1C2SC3=NC=NN3C=2C=C[CH:16]=1.N1N2C(S[C:32]3C=CC=C[C:33]=32)=NC=1.ClC1C2SC3=NC=NN3C=2C=CC=1.COC1C2SC3=NC=NN3C=2C=CC=1.CC1N=C2SC3C(C)=CC=CC=3N2N=1>>[CH2:15]([C:12]1[N:11]=[C:8]2[S:9][C:10]3[CH:2]=[C:3]([CH2:32][CH3:33])[CH:4]=[CH:5][C:6]=3[N:7]2[N:13]=1)[CH3:16]

Participants

7

Reactant 6

HCID 20368090HCID 20368090, compoundHCID 20368103HCID 20368103, compoundHCID 20368106HCID 20368106, compoundHCID 20368121HCID 20368121, compoundHCID 20368123HCID 20368123, compoundHCID 57056129HCID 57056129, compound

Product 1

HCID 20368120HCID 20368120, compound

Procedure

The preferred compounds of this invention are 5-methyl-s-triazolo[5,1-b]benzothiazole, 5-fluoro-s-triazolo[5,1-b]-benzothiazole, s-triazolo[5,1-b]benzothiazole, 5-chloro-s-triazolo[5,1-b]benzothiazole, 5-methoxy-s-triazolo[5,1-b]benzothiazole, and 2,5-dimethyl-s-triazolo[5,1-b]benzothiazole.

Sources & evidence

ORD record
ord-a849448b64ec47138dbc9c3862712bf1
Source dataset
uspto-grants-1976_08
Patent number
US03974286

Reaction notes

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