HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 10207696, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 10300352 | HCID 10300352 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10207696 | HCID 10207696 | — |
Reaction Steps
N-[3,3-Dimethyl-1-(4-piperidylmethyl)indolin-6-yl][2-(1H-indazol-6-ylamino)(3-pyridyl)]carboxamide (140 mg, Example 41) was dissolved in 10 mL EtOH. Formaldehyde (10 mL, 37%) was added, followed by 100 mg of NaCNBH3. The mixture was stirred at RT overnight, and concentrated in vacuo. The crude was extracted between saturated NaHCO3 solution and EtOAc, the resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo to afford a yellow solid. This material was further purified by preparative HPLC to yield a white solid. MS: 510 (M+1). Calc'd. for C30H35N7O−509.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514564B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-d1fec9b9cb744f1a81cfaabc90f0a1a4 |
| Source note | uspto-grants-2009_04 |