HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-tert-Butyl-phenyl)-4-piperidin-4-yl-benzamide → (1R,2R)-2-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-phenyl]-piperidine-1-carbonyl}-cyclopentanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3-tert-Butyl-phenyl)-4-piperidin-4-yl-benzamide | HCID 59317976 | — |
| Reactant | (1S,2S)-2-{4-[5-(3-tert-butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclopentanecarboxylic acid | HCID 59317991 | — |
| Reactant | (1s,2s)-2-(Benzyloxycarbonyl)cyclopentanecarboxylic acid | HCID 66738585 | — |
| Product | (1R,2R)-2-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-phenyl]-piperidine-1-carbonyl}-cyclopentanecarboxylic acid | HCID 59318034 | — |
Reaction Steps
(1R,2R)-2-{4-[4-(3-tert-Butyl-phenylcarbamoyl)-phenyl]-piperidine-1-carbonyl}-cyclopentanecarboxylic acid was synthesized from (1S,2S)-cyclopentane-1,2-dicarboxylic acid monobenzyl ester and N-(3-tert-butyl-phenyl)-4-piperidin-4-yl-benzamide in a manner similar to the one described in the synthesis of (1S,2S)-2-{4-[5-(3-tert-butyl-phenylcarbamoyl)-pyridin-2-yl]-piperazine-1-carbonyl}-cyclopentane-carboxylic acid above. LCMS calcd for C29H36N2O4 (m/e) 476, obsd 477 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08324385B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-dc7396bc5ad742fca2ea22ea68140c4d |
| Source note | uspto-grants-2012_12 |