HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25649Generated: October 30, 2026
N-Methylpropylamine → HCID 178457210, compound
https://huagongshe.com/reaction/25649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylpropylamine | HCID 12315 | — |
| Reactant | HCID 178484794 | HCID 178484794 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178457210 | HCID 178457210 | 47.3% |
Reaction Steps
320 mg (corresponds to 0.59 mmol) of crude trans-N-[4-(5-Iodo-pent-1-ynyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide in 6 ml MeOH was treated with 0.6 ml (5.93 mmol) of N-methylpropylamine. The reaction was stirred overnight at 65° C. and partitioned between aqueous 1N NaOH /Et2O (3×), the organic phases were dried over Na2SO4 and evaporated. Purification by flash column chromatography on silica gel (CH2Cl2, then CH2Cl2/MeOH 95:5 to 9:1) gave 128 mg (47% over two steps) of trans-N-Methyl-N-{4-[5-(methyl-propyl-amino)-pent-1-ynyl]-cyclohexyl}-4-trifluoromethyl-benzenesulfonamide, MS: 459 (MH+). The following compounds can be obtained in analogy:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06858651B2 |
|---|
| Source dataset | uspto-grants-2005_02 |
|---|
| ORD ID | ord-5e62d54e190a458e8ae513f47a3c8f7b |
|---|
| Source note | uspto-grants-2005_02 |
|---|