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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505193Generated: October 31, 2026

Ammonia → (8-Carbamoylmethyl-7-chloro-naphthalen-2-ylmethyl)-(2-fluoro-ethyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/505193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant(7-{[Tert-butoxycarbonyl-(2-fluoro-ethyl)-amino]-methyl}-2-chloro-naphthalen-1-yl)-acetic acidHCID 86625785—
SolventDimethylformamideHCID 6228—
Product(8-Carbamoylmethyl-7-chloro-naphthalen-2-ylmethyl)-(2-fluoro-ethyl)-carbamic acid tert-butyl esterHCID 86625784—

Reaction Steps

Carbonyl diimidazole (95 mg, 0.58 mmol) was added at RT under an atmosphere of argon to a solution of (7-{[tert-butoxycarbonyl-(2-fluoro-ethyl)-amino]-methyl}-2-chloro-naphthalen-1-yl)-acetic acid (210 mg, 0.53 mmol) in DMF (2.0 ml). After 2 h at RT, concentrated aqueous ammonia (4.3 ml) is added, and the mixture is stirred for 15 minutes at RT. The emulsion is extracted with EtOAc. The organic layer is washed with brine and dried over Na2SO4. After concentration, the residue is purified by FCC (EtOAc) to yield the title compound. 1H NMR (d6-DMSO, 400 MHz): δ 1.38+1.46 (2x br s, 9H), 3.3-3.6 (br m, 2H), 4.08 (s, 2H), 4.40-4.65 (br m, 2H), 4.61 (s, 2H), 7.02 (br s, NH), 7.42 (br d, J=9 Hz, 1H), 7.48-7.58 (br m, 3H), 7.80-7.90 (br m, 2H), 7.95 (br d, J=9 Hz, 1H). ES+-MS: 412.3, 414.2 [M+H+H2O]+. ES−-MS: 393.3, 395.3 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781438B2
Source datasetuspto-grants-2010_08
ORD IDord-cd372720ef6c4cf1bf33e03c412da0bf
Source noteuspto-grants-2010_08