HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Isopropylpiperidin-4-ol → 5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Isopropylpiperidin-4-ol | HCID 79681 | — |
| Reactant | Ethyl 5-hydroxy-1H-indole-2-carboxylate | HCID 90677 | — |
| Reactant | 5-(1-Isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid ethyl ester | HCID 44185246 | — |
| Product | 5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid | HCID 59699456 | — |
Reaction Steps
According to the procedure described for the synthesis of Example 5/step 1 5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid ethyl ester was synthesized from 5-hydroxy-1H-indole-2-carboxylic acid ethyl ester (commercially available) and 1-isopropyl-piperidin-4-ol (commercially available). The title compound was yielded in 33% as off-white solid. MS (m/e): 331.1 (MH+, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07361682B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-3107c198f75b46f3b75c499866bceb56 |
| Source note | uspto-grants-2008_04 |