HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204346Generated: October 31, 2026
1,3-Dimethyl-1H-pyrazol-5-amine → HCID 86703149, compound
https://huagongshe.com/reaction/2204346
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dimethyl-1H-pyrazol-5-amine | HCID 520721 | — |
| Reactant | 1-Chloro-N,N-2-trimethylpropenylamine | HCID 640792 | — |
| Reactant | 5-Amino-3-chloro-1-methyl-1,2-dihydropyridin-2-one | HCID 71756073 | — |
| Reactant | 5-bromo-2-[(4-chloro-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid methyl ester | HCID 86703101 | — |
| Reactant | HCID 86703150 | HCID 86703150 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86703149 | HCID 86703149 | — |
Reaction Steps
The title compound was prepared in analogy to the procedure described for Intermediate AW but in the step corresponding to Step AW2, 5-bromo-2-[(4-chloro-3-fluoro-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid methyl ester (Step AZ1) and 5-amino-3-chloro-1-methyl-1H-pyridin-2-one (Step E5) were used instead of 5-bromo-2-[(4-chloro-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid methyl ester and 2,5-dimethyl-2H-pyrazol-3-ylamine respectively. Moreover, in this step, the procedures described for Steps H3 and H2 using 1-chloro-N,N,2-trimethylpropenylamine and Et3N were used. The title compound (containing some of the corresponding 2-chloro analog) was obtained as a white foam. tR: 1.18 min (HPLC 3); ESI-MS: tR=1.10 min, [M+H]+ 512/514/516 (LC-MS 1); TLC: Rf=0.19 (EtOAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365576B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-0d0db51949ec4d19b94ec82c47c6bae8 |
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| Source note | uspto-grants-2016_06 |
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