HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-methyl-2-pyrrolidone → Methyl 4-[5-[(hydroxy)-(1-methyl-2-oxopyrrolidin-3-yl)methyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Methyl 4-(5-formyl-1-methylindol-3-ylmethyl)-3-methoxybenzoate | HCID 14882555 | — |
| Product | Methyl 4-[5-[(hydroxy)-(1-methyl-2-oxopyrrolidin-3-yl)methyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoate | HCID 19823230 | — |
Reaction Steps
Using a similar procedure to that described in Example 1, part d, except starting from methyl 4-(5-formyl-1-methylindol-3-ylmethyl)-3-methoxybenzoate and N-methylpyrrolidone, methyl 4-[5-[(hydroxy)-(1-methyl -2-oxopyrrolidin-3-yl)methyl]-1-methylindol-3-ylmethyl]-3-methoxybenzoate was obtained (40%) as a foam; NMR (300 MHz, DMSO-d6): 1.43-1.65 (m, 1.5H), 1.95 (m, 0.5H), 2.40-2.60 (m, 2.5H), 2.65-2.80 (m, 2H), 2.90-3.25 (m, 1.5H), 3.70 (s, 3H), 3.83 (s, 3H), 3.85-4.08 (m, 5H), 4.92 (d, 0.5H), 5.17 (s, 0.5H), 7.0-7.55 (m, 7H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05047402 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-ba796a82c9c4435b96bc131b7c79be9b |
| Source note | uspto-grants-1991_09 |