HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bis-(2-chloro-ethyl)-(4-methoxy-benzyl)-amine → 4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperidine-4-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bis-(2-chloro-ethyl)-(4-methoxy-benzyl)-amine | HCID 415290 | — |
| Reactant | Ethyl{[4-(2-butynyloxy)phenyl]sulfonyl}acetate | HCID 11335441 | — |
| Product | 4-(4-But-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperidine-4-carboxylic acid ethyl ester | HCID 11363756 | — |
Reaction Steps
4-(4-but-2-ynyloxy-benzenesulfonyl)-1-(4-methoxy-benzyl)-piperidine-4-carboxylic acid ethyl ester was prepared according to the general method as outlined in Example 1. Starting from (4-but-2-ynyloxy-benzenesulfonyl)-acetic acid ethyl ester (2 g, 6.73 mmol) and bis-(2-chloro-ethyl)-(4-methoxy-benzyl)-amine (2.61 g, 8.75 mmol) and following the procedure as outlined in Example 1 (Step 6) 2.5 g of the product was isolated. Yield 2.5 g (77%); yellow oil; MS: 486 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06753337B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-16fbafb10611453d85bd73db29f4c9dc |
| Source note | uspto-grants-2004_06 |