HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 69296792, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate | HCID 2734674 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 21985053 | HCID 21985053 | — |
| Product | Dichloromethane methanol ammonium hydroxide | HCID 21896990 | — |
| Product | HCID 69296792 | HCID 69296792 | 30% |
Reaction Steps
Using General Procedure B: To a stirred solution of (1H-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (148 mg, 0.53 mmol) and N-tert-butoxycarbonyl-L-prolinal (110 mg, 0.55 mmol) in CH2Cl2 (5 mL) was added NaBH(OAc)3 (146 mg, 0.69 mmol) and the resultant mixture was stirred at room temperature overnight. Purification of the crude material by radial chromatography on silica gel gel (2 mm plate, 50:1:1 CH2Cl2/MeOH/NH4OH then 10:1:1 CH2Cl2/MeOH/NH4OH) afforded the desired amine (73 mg, 30%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354932B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-c89663fd66924e66a1199401cee4ffe3 |
| Source note | uspto-grants-2008_04 |