HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 4-(3-iodo-2-{2-[(2R)-2-methyl-1-pyrrolidinyl]ethyl}-1-benzofuran-5-yl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Benzonitrile, 4-(2-(2-((2r)-2-methyl-1-pyrrolidinyl)ethyl)-5-benzofuranyl)- | HCID 9818903 | — |
| Product | 4-(3-iodo-2-{2-[(2R)-2-methyl-1-pyrrolidinyl]ethyl}-1-benzofuran-5-yl)benzonitrile | HCID 67534215 | 18% |
Reaction Steps
The mono-(L)-tartaric acid salt of the product of Example 1D and N-iodosuccinimide were processed as in Example 156, except that a large excess of N-iodosuccinimide (2.4 molar equivalents) was utilized, to provide the title compound as a tan gum (18% yield). MS (ESI) m/z 457 (M+H)+; 1HNMR (300 MHz, CD3OD) δ 1.49 (d, 3 H), 1.67-1.84 (m, 1 H), 2.00-2.25 (m, 2 H), 2.29-2.44 (m, 1 H), 3.22-3.63 (m, 5 H), 3.72-3.91 (m, 2 H), 7.59-7.64 (m, 2 H), 7.72 (dd, 1 H), 7.80-7.89 (m, 4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969730B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-38c72475dc624e74aa1cf00688b2538d |
| Source note | uspto-grants-2005_11 |