HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-(5-((2r)-1-Methylpyrrolidin-2-yl)thien-2-yl)-1h-benzimidazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-(5-((2r)-Pyrrolidin-2-yl)thien-2-yl)-1h-benzimidazole-4-carboxamide | HCID 66760237 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(5-((2r)-1-Methylpyrrolidin-2-yl)thien-2-yl)-1h-benzimidazole-4-carboxamide | HCID 66758802 | — |
Reaction Steps
A solution of EXAMPLE 16D (50 mg) in methanol (20 mL) was treated with 37 wt % formaldehyde in water (114 μL) and stirred overnight. Sodium cyanoborohydride (315 mg) was added, and the solution was stirred for 3 hours and concentrated. The concentrate was dissolved in methanol and TFA, and purified by HPLC (Zorbax C-8, 0.1% TFA/acetonitrile/water). 1H NMR (CD3OD) δ 2.30 (m, 2H), 2.47 (m, 1H), 2.74 (m, 1H), 2.94 (s, 3H), 3.31-3.40 (m, 1H), 3.88 (m, 1H), 4.81 (m, 1H), 7.40 (t, J=7.7 Hz, 1H), 7.51 (d, J=3.7 Hz, 1H), 7.73 (d, J=7.6 Hz, 1H), 7.86 (d, J=4.0 Hz, 1H), 7.95 (d, J=7.6 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08067613B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-361845f7a3cd442ea76248c3db346514 |
| Source note | uspto-grants-2011_11 |