HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(3-Fluoro-4-isocyanato-phenyl)-2-methyl-propionic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 2-(4-Amino-3-fluoro-phenyl)-2-methyl-propionic acid methyl ester | HCID 68645804 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-Fluoro-4-isocyanato-phenyl)-2-methyl-propionic acid methyl ester | HCID 86640268 | — |
Reaction Steps
In analogy to the procedure described in example 9.1, 2-(4-amino-3-fluoro-phenyl)-2-methyl-propionic acid methyl ester (Chung, Jae-Uk; Kim, Su Yeon; Lim, Ju-Ok; Choi, Hyun-Kyung; Kang, Sang-Uk; Yoon, Hae-Seok; Ryu, HyungChul; Kang, Dong Wook; Lee, Jeewoo; Kang, Bomi; Choi, Sun; Toth, Attila; Pearce, Larry V.; Pavlyukovets, Vladimir A.; Lundberg, Daniel J.; Blumberg, Peter M. Bioorganic & Medicinal Chemistry (2007), 15(18), 6043-6053) was reacted with triphosgene in the presence of Et3N in CH2Cl2 under reflux conditions for 16 h to give the title compound as brown oil which was used in the next step without further purification. MS: m/e=255.4 [M+NH4+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153663B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-ff8243a44e794774b82e12c79a710500 |
| Source note | uspto-grants-2012_04 |