HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 21064711, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21064712 | HCID 21064712 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21064711 | HCID 21064711 | 99.5% |
Reaction Steps
6-(2-tert-Butoxycarbonylamino-acetyl)-nicotinic acid methyl ester (132.7 mg, 0.451 mmol) was dissolved into 3 mL of MeOH. To this was added sodium borohydride (18.96 mg, 0.50 mmol) in one portion. After 0.5 h, the reaction mixture was concentrated on a rotary evaporator. The residue was dissolved into 20 mL of EtOAc. The organic phase was washed with 2×20 mL NH4Cl and 1×20 mL of brine, dried (MgSO4) filtered and concentrated to give 133 mg, 99.5% of 6-(2-tert-butoxycarbonylamino-1-hydroxy-ethyl)-nicotinic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07119102B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-6d4818735b744cb68167d936f55ff984 |
| Source note | uspto-grants-2006_10 |