HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-[(4-Dipropylaminobutyl)methylamino]methylbenzonitrile → HCID 67316320, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-[(4-Dipropylaminobutyl)methylamino]methylbenzonitrile | HCID 16117293 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67316320 | HCID 67316320 | 99% |
Reaction Steps
100 mg (0.33 mmol) of unpurified 4-[(4-dipropylaminobutyl)methylamino]methylbenzonitrile (2b) synthesized in Example 5 was charged in a 25 ml recovery flask, and dissolved in 3 ml of methanol. After 290 mg (0.80 mmol, 2.4 equivalents) of a 10% hydrochloric acid-methanol solution was added dropwise to the solution under cooling with ice, the mixture was stirred for one hour. The reaction solution was then concentrated. After the addition of 5 ml of methanol to the residue, the mixture was reconcentrated. This operation was repeated twice, thereby obtaining 122 mg of 4-[(4-dipropylaminobutyl)methylamino]methylbenzonitrile hydrochloride (2ba) as a colorless oily substance (yield: 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977512B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-d7a08052f2da4faeb68b8d86c91eaadd |
| Source note | uspto-grants-2011_07 |