Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | HCID 19387332 | HCID 19387332 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178464051 | HCID 178464051 | 87.1% |
Reaction Steps
0.100 g (0.148 mmol) 2-[2-(diethylamino)-ethyl]-5-[[2-(diethylamino)ethyl]amino]-7,10-bis(phenylmethoxy)-anthra[1,9-cd]pyrazol- 6(2H)-one is dissolved in cold, dry dichloromethane (4 ml) and boron trichloride (4 ml, 1M solution in dichloromethane) is added dropwise over 30 minutes under argon. The reaction mixture is maintained at 0°-5° C. for 1 hour and then treated dropwise with cold methanol under argon. The mixture is then maintained at room temperature for 2 hours and then evaporated to dryness in vacuo. The resulting crude hydrochloride salt is dissolved in a minimum volume of methanol and then chromatographed on a column of silica gel (60A) using an eluting solvent of dichloromethane:methanol (80:20 v/v) and then dichloromethane:methanol:triethylamine (80:20:1 v/v). The major red band is collected and evaporated in vacuo to yield 0.060 g of the title compound as an orange-red solid, m.p. 152° C.; λmax (methanol) (E/cm/M) 520 nm (22000).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05447950 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-026f6283fccb482cadf45ab2fd62f8f3 |
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| Source note | uspto-grants-1995_09 |
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