HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 22310861, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 22310882 | HCID 22310882 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22310861 | HCID 22310861 | 67% |
Reaction Steps
Sodium cyanoborohydride (0.2 g) was added in a single portion to methyl N-(3,4-dichlorobenzyl)-5-aminoindole-2-carboxylate (0.16 g), ethyl glyoxalate (0.2 ml of 50 wt % solution in toluene) and acetic acid (0.1 ml) in methanol (3 ml). The reaction was stirred for 5 mins then partitioned between ethyl acetate and 2M HCl. Combined organic extracts were dried (MgSO4) and concentrated to give an oil which crystallised upon trituration with i-hexane. Filtration yielded the desired end product as an off-white powder (0.136 g, 67%); NMR δ(CD3SOCD3) 1.18 (t, 3H), 3.79 (s, 3H), 3.82 (d, 2H), 4.08 (q, 2H), 5.72 (s, 2H), 6.60-7.50 (m, 7H); M/z (+) 435 (M+), 133.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441004B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-189944261a8b4d7f892a7c249c2d8f8f |
| Source note | uspto-grants-2002_08 |