HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417968Generated: November 3, 2026
Sodium borohydride → 5-benzyloxy-3-hydroxymethyl-4-methoxymethyl-9-{2-[N-methyl-N-(2-phenylethyl)-amino]-2-oxoethyl}-9H-pyrido[3,4-b]indole
https://huagongshe.com/reaction/1417968
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-benzyloxy-4-methoxymethyl-9-{2-[N-methyl-N-(2-phenylethyl)-amino]-2-oxoethyl}-9H-pyrido[3,4-b]indole-3-carbaldehyde | HCID 86753861 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-benzyloxy-3-hydroxymethyl-4-methoxymethyl-9-{2-[N-methyl-N-(2-phenylethyl)-amino]-2-oxoethyl}-9H-pyrido[3,4-b]indole | HCID 67695850 | 96.8% |
Reaction Steps
25 mg of sodium borohydride is added to a solution of 35 mg of 5-benzyloxy-4-methoxymethyl-9-{2-[N-methyl-N-(2-phenylethyl)-amino]-2-oxoethyl}-9H-pyrido[3,4-b]indole-3-carbaldehyde in 1 ml of tetrahydrofuran at 0° C., and it is then stirred for 3 hours at 0° C. Then, the reaction mixture is poured into ice water and extracted three times with ethyl acetate. The organic phase is dried on magnesium sulfate, filtered and concentrated by evaporation in a vacuum. 34 mg of 5-benzyloxy-3-hydroxymethyl-4-methoxymethyl-9-{2-[N-methyl-N-(2-phenylethyl)-amino]-2-oxoethyl}-9H-pyrido[3,4-b]indole is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05880126 |
|---|
| Source dataset | uspto-grants-1999_03 |
|---|
| ORD ID | ord-35b9fc0bf2f94967b769064e45784d78 |
|---|
| Source note | uspto-grants-1999_03 |
|---|