HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971007Generated: October 28, 2026
Binap, (A+-)- → 7-Chloro-1-{[(7R,8R)-7-methyl-1,4-dioxaspiro[4.5]dec-8-yl]amino}-5H-pyrido[4,3-b]indole-4-carbonitrile
https://huagongshe.com/reaction/1971007
Participants
| Role | Name | HCID | Charge |
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| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 1,7-dichloro-5H-pyrido[4,3-b]indole-4-carbonitrile | HCID 56595057 | — |
| Reactant | (7R,8R)-7-Methyl-1,4-dioxaspiro[4.5]decan-8-amine | HCID 59543149 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Chloro-1-{[(7R,8R)-7-methyl-1,4-dioxaspiro[4.5]dec-8-yl]amino}-5H-pyrido[4,3-b]indole-4-carbonitrile | HCID 68669252 | — |
Reaction Steps
A flask containing 1,7-dichloro-5H-pyrido[4,3-b]indole-4-carbonitrile (Example 1 Step 4, 140 mg, 0.53 mmol), BINAP (50 mg, 0.08 mmol), Pd2(dba)3 (24 mg, 0.03 mmol), and NaOtBu (164 mg, 1.71 mmol) was evacuated and refilled with nitrogen (×3). Degassed DME (10 mL) and (7R,8R)-7-methyl-1,4-dioxaspiro[4.5]decan-8-amine (183 mg, 1.07 mmol) were added to the mixture. The reaction mixture was heated to 85° C. overnight, cooled to room temperature, diluted with EtOAc, and washed with water and brine. The organic layer was dried (sodium sulfate), concentrated, and purified by flash chromatography to afford the title compound. LRMS (APCI) calc'd for (C21H21ClN4O2) [M+H]+, 397.1. found 397.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431569B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-685499e26cfa407c87364e0b8faabfc1 |
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| Source note | uspto-grants-2013_04 |
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