HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 9-[2-(1-Piperidinyl)ethyl]-2,4-di-1-pyrrolidinyl-9H-pyrimido[4,5-b]indole monohydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 9-[2-(1-Piperidinyl)ethyl]-2,4-di-1-pyrrolidinyl-9H-pyrimido[4,5-b]indole | HCID 19064085 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 9-[2-(1-Piperidinyl)ethyl]-2,4-di-1-pyrrolidinyl-9H-pyrimido[4,5-b]indole monohydrochloride | HCID 86753032 | — |
Reaction Steps
A mixture of 9-[2-(1-piperidinyl)ethyl]-2,4-di-1-pyrrolidinyl-9H-pyrimido[4,5-b]indole (I, EXAMPLE5, 44 g) and aqueous hydrochloric acid (1M, 107 mL) in ethanol (900 mL) is stirred at 60° until the mixture becomes homogeneous. The mixture is concentrated under reduced pressure in a stream of nitrogen. When the reaction volume reaches approximately half of the original volume, crystallization begins. The mixture is cooled to -10° for 3 hr and the title compound, is isolated by filtration, mp >260°; NMR (CDCl3) 7.88, 7.52, 7.28, 7.13, 4.86, 3.94-3.89, 3.62, 3.45, 3.15 and 2.01-1.96 δ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05795986 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-199952f5055741159255ff7ebe7f467f |
| Source note | uspto-grants-1998_08 |