HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220881Generated: November 3, 2026
N-Methylbutylamine → HCID 135735998, compound
https://huagongshe.com/reaction/220881
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylbutylamine | HCID 8068 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 136128376 | HCID 136128376 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 135735998 | HCID 135735998 | — |
Reaction Steps
A solution of 1-{3-[2-methyl-4-(3-methyl-4,10-dihydro-3H-2,3,4,9-tetraaza-benzo[f]azulene-9-carbonyl)-phenyl]-propionyl}-piperidine-4-carbaldehyde from Example E58.1 (2.43 mg, 0.005 mmol) in 1,2-dichloroethane (0.05 ml) was added to a solution of butyl-methyl-amine (0.43 mg, 0.005 mmol) in 1,2-dichloroethane (0.05 ml) and the mixture was heated at 50° C. for 3 h then stirred at room temperature for 2 days. A solution of sodium tri-acetoxyborohydride (1.59 mg, 0.0075 mmol) in DMF (0.05 ml) was added and the mixture was stirred for 20 h at room temperature. Solvents were removed in vacuo to yield the title compound. MS: (ESI)+:[M+H]+=557.6
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202858B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-895df675030647f4ae4d62367e8a581f |
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| Source note | uspto-grants-2012_06 |
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