Ammonia → HCID 21255046, compound

HRID 636426Notes

Reaction equation

HRID 636426 reaction equation
Cl[C:2]1[N:7]2[N:8]=[C:9]([S:20][CH3:21])[C:10]([S:11]([C:14]3[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=3)(=[O:13])=[O:12])=[C:6]2[N:5]=[C:4]([CH3:22])[CH:3]=1.[NH3:23]>CO>[CH3:22][C:4]1[CH:3]=[C:2]([NH2:23])[N:7]2[N:8]=[C:9]([S:20][CH3:21])[C:10]([S:11]([C:14]3[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=3)(=[O:13])=[O:12])=[C:6]2[N:5]=1

Participants

4

Reactant 2

HCID 222AmmoniaHCID 21254972HCID 21254972, compound

Product 1

HCID 21255046HCID 21255046, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

In an analogous manner to that described in Example 4), from 7-chloro-5-methyl-2-methylsulphanyl-3-(pyridine-3-sulphonyl)-pyrazolo[1,5-a]pyrimidine and NH3 in MeOH there was obtained 5-methyl-2-methylsulphanyl-3-(pyridine-3-sulphonyl) -pyrazolo[1,5-a]pyrimidin-7-ylamine as colorless crystals, m.p. 226.8 -227.5°.

Sources & evidence

ORD record
ord-7d0c1aecaa3b4f92b5b3a22ee9a0d053
Source dataset
uspto-grants-2001_02
Patent number
US06194410B1

Reaction notes

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