HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole-5-carboxaldehyde → HCID 45272332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole-5-carboxaldehyde | HCID 589040 | — |
| Reactant | HCID 45139978 | HCID 45139978 | — |
| Product | HCID 45272332 | HCID 45272332 | 32.5% |
Reaction Steps
Compound 40b was prepared according to Procedure A using 39a (65 mg, 0.20 mmol) and indole-5-carboxaldehyde (35 mg, 0.24 mmol) to give 40b (29 mg, 32%) after column chromatography. 1H NMR (400 MHz, CDCl3) δ 0.84 (t, 3H, J=7.2 Hz), 1.33-1.44 (m, 3H), 1.85 (d, 1H, J=10.0 Hz), 2.41-2.82 (m, 19H), 3.60 (s, 2H), 6.35 (d, 1H, J=2.0 Hz), 6.49-6.58 (m, 2H), 6.85 (d, 1H, J=8.4 Hz), 7.14-7.20 (m, 2H), 7.31 (d, 1H, J=8.4 Hz), 7.54 (s, 1H), 8.38 (bs, 1H). The free base of 40b was converted into oxalate salt. m.p. 198-203° C. Anal. [C28H38N4O.2.5(COOH)2.3H2O]C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034877B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-989945a79d9044489edf4a58e023b0e3 |
| Source note | uspto-grants-2015_05 |