HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 71748042, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Bromopyrazolo[1,5-a]pyrimidine-2-carboxylic acid | HCID 771938 | — |
| Reactant | 2-Chloro-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine--hydrogen chloride (1/1) | HCID 53438318 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 71748042 | HCID 71748042 | — |
Reaction Steps
To 0.03 g (0.12 mmol) 6-bromo-pyrazolo[1,5-A]pyrimidine-2-carboxylic acid, 0.12 mmol 2-chloro-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine hydrochloride and 0.51 mmol triethyl amine (TEA) in 1.5 ml dimethylformamide (DMF) 0.14 mmol TBTU (O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate) was added and the reaction mixture was stirred at RT for 1 h. Water was added to the reaction mixture. The precipitate was collected and dried. Yield: 0.018 g (36% of theory). ESI-MS: m/z=406 (M+H)+; Rt(HPLC): 1.29 min. (Method J).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029360B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-7b896e8e08564d0e923105eb2cce194d |
| Source note | uspto-grants-2015_05 |