HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611099Generated: October 30, 2026
Diisopropylethylamine → HCID 9958698, compound
https://huagongshe.com/reaction/1611099
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1H-Indole-6-carboxaldehyde | HCID 2773435 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 11711108 | HCID 11711108 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 9958698 | HCID 9958698 | 64.3% |
Reaction Steps
1H-indole-6-carbaldehyde (238 mg, 1.64 mmol, 1.36 equiv) [Moyer, Mikel P.; Shiurba, John F.; Rapoport, Henry; J. Org. Chem.; 1986, 51, 5106-5110] was added to the solution of the 2-[5-(3,4-dimethoxy-phenyl)-pyrimidin-2-ylsulfanyl]-N-piperidin-3-ylmethyl-acetamide 1h (TFA)n (1.20 mmol, obtained from step 6) and diisopropylethylamine (0.85 mL, 4.8 mmol, 4 equiv) in 50 mL dichloroethane. Sodium triacetoxyborohydride (0.47 g, 2.24 mmol, 1.8 equiv) was added to the solution and the resulting suspension was stirred vigorously overnight. Methanol (5 mL) was added to quench the reaction. The mixture was concentrated and the residue was diluted with ethyl acetate. The solution was poured into saturated NaHCO3 solution (40 mL) and extracted with EtOAc. The combined organic phases were washed with brine, dried (Na2SO4), and concentrated. Chromatography on silica gel (10% methanol in chloroform) afforded 2-[5-(3,4-dimethoxy-phenyl)-pyrimidin-2-ylsulfanyl]-N-[1-(1H-indol-6-ylmethyl)-piperidin-3-ylmethyl]-acetamide (free base, 410 mg, 64%) as a light tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06984643B2 |
|---|
| Source dataset | uspto-grants-2006_01 |
|---|
| ORD ID | ord-8f6715a2eeea41b2a1fc18a697f1497d |
|---|
| Source note | uspto-grants-2006_01 |
|---|