Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydride | HCID 166653 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 68914665 | HCID 68914665 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25256747 | HCID 25256747 | — |
Reaction Steps
A solution of 3-ethyl-8H-3a-aza-cyclopenta[a]indene-1,2-dicarboxylic acid dimethyl ester (2.5 g, 8.35 mmol) in anhydrous dichloromethane (30 mL) was added dropwise to a stirred suspension of LiAlH4 (0.793 g, 20.87 mmol) in anhydrous ether (30 mL) at 0° C. The mixture was stirred for 15 min after the addition was completed. The excess hydride was carefully decomposed by the slow, sequential addition of water (1.3 mL), 15% NaOH aqueous solution (1.3 mL), and water (3.6 mL). The solid inorganic salt was filtered and washed with dichloromethane. The combined filtrate and washings was concentrated in vacuo to dryness. The solid residue was triturated with ether, collected the solid product by filtration, and dried in vacuo to yield (3-ethyl-2-hydroxymethyl-8H-3a-azacyclopenta[a]inden-1-yl)-methanol (DA-1099), 1.31 g (64%): mp 131-133° C.; 1H NMR (DMSO-d6) δ 1.18 (3H, t, J=7.3 Hz, Me), 2.89 (2H, q, J=7.3 Hz, CH2), 3.81 (2H, s, CH2), 4.36 (2H, d, J=5.2, CH2O), 4.45 (2H, d, J=5.2 Hz, CH2O), 4.47 (1H, t, J=5.2 Hz, exchangeable, OH), 4.63 (1H, t, J=5.2 Hz, exchangeable, OH), 7.06-7.09 (1H, m, ArH), 7.30-7.34 (1H, m, ArH), 7.37-7.39 (1H, m, ArH), 7.45-7.46 (1H, m, ArH). Anal. Calcd for C15H17NO2: C, 74.05; H, 7.04; N, 5.76. Found: C, 73.22; H, 6.94; N, 5.71.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08410130B2 |
|---|
| Source dataset | uspto-grants-2013_04 |
|---|
| ORD ID | ord-fcda781827aa4db5ac4df3e2bcec6339 |
|---|
| Source note | uspto-grants-2013_04 |
|---|