HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenamine, 3-chloro-, hydrochloride (1:1) → HCID 178452690, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenamine, 3-chloro-, hydrochloride (1:1) | HCID 67336 | — |
| Reactant | HCID 178484263 | HCID 178484263 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178452690 | HCID 178452690 | — |
Reaction Steps
With the exclusion of air, 172 mg (1.05 mmol) of 3-chloro-aniline hydrochloride (see Step 14.4) are added to 248 mg (0.70 mmol) of N'-[3-(4-tert-butoxycarbonylamino-phenyl)-4-cyano-1H-pyrazol-5-yl]-N,N-dimethylformamidine in 2 ml of methanol and the reaction mixture is boiled for 19 hours. The reaction mixture is then concentrated by evaporation and chromatographed (SiO2, methylene chloride/ethanol [20:1]). Stirring with diethyl ether/hexane yields 3-(4-tert-butoxycarbonylamino-phenyl)-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine; m.p. 165-168° C. (decomposition); FAB-MS: (M)+= 436; HPLC: TRet (Grad20-100)=15.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981533 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-b8cfb2af3c96492cb891c292fbf50d94 |
| Source note | uspto-grants-1999_11 |