HuagongsheHuagongshe Chemistry Print Report · For research reference only
{4-[4-(3-Carbamoylpropylamino)phenyl]butyl}carbamic acid tert-butyl ester → 4-[4-(4-Aminobutyl)phenylamino]butyramide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | {4-[4-(3-Carbamoylpropylamino)phenyl]butyl}carbamic acid tert-butyl ester | HCID 58664823 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | 4-[4-(4-Aminobutyl)phenylamino]butyramide | HCID 58664835 | — |
Reaction Steps
{4-[4-(3-Carbamoylpropylamino)phenyl]butyl}carbamic acid tert-butyl ester 430 (0.23 g, 0.66 mmol) was cooled to 0° C. in an ice bath. A cold solution of TFA/dichloromethane (10 mL) was added. The reaction was slowly warmed to room temperature and stirred for 30 minutes. The solvent was evaporated in vacuo to provide 440. 1H NMR (300 MHz, CD3OD) δ 1.69 (m, 4H), 1.95 (m, 2H), 2.47 (m, 2H), 2.71 (m, 2H), 2.93 (m, 2H), 3.39 (m, 2H), 7.39 (s, 4H). m/z (ESI) 250.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07875619B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-06f20629399a42e6b57a46d70182a8f2 |
| Source note | uspto-grants-2011_01 |