HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636441Generated: October 29, 2026
N,N-Dimethylethylenediamine → HCID 21254927, compound
https://huagongshe.com/reaction/636441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | HCID 21255038 | HCID 21255038 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21254927 | HCID 21254927 | 48% |
| Product | HCID 21255024 | HCID 21255024 | 17% |
Reaction Steps
0.26 g (3 mmol) of 2-dimethylaminoethylamine in 5 ml of DMF was added to a solution of 0.4 g (1 mmol) of 3-benzenesulphonyl-5-chloro-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidin-7-ylamine in 10 ml of DMF and stirred at 90° for 1 hr. The reaction solution was evaporated and the residue was partitioned between H2O and CH2Cl2. The aqueous phase was extracted three times with 50 ml of CH2Cl2. The combined organic phases were dried (MgSO4), filtered and evaporated. Subsequent chromatography (silica gel, CH2Cl2/MeOH 8:1) yielded 0.20 g (48%) of 3-benzenesulphonyl-N5,N5-dimethyl-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidine-5,7-diamine as colorless crystals, m.p.>230°, and 0.08 g (17%) of 3-benzenesulphonyl-N5-(2-dimethylamino-ethyl)-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidine-5,7-diamine as colorless crystals, m.p. 210-212°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06194410B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-9335b5035d04408bb23621c79897b699 |
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| Source note | uspto-grants-2001_02 |
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