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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622011Generated: October 24, 2026

Hydrochloric Acid → Tert-butyl 5-amino-2-chloropyridin-3-ylcarbamate

https://huagongshe.com/en/reaction/1622011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-butyl 2-chloro-5-(diphenylmethyleneamino)pyridin-3-ylcarbamateHCID 86647087—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 5-amino-2-chloropyridin-3-ylcarbamateHCID 86647086—

Reaction Steps

To a solution of tert-butyl 2-chloro-5-(diphenylmethyleneamino)pyridin-3-ylcarbamate (0.280 g, 0.686 mmol) in THF (5 mL) was added hydrochloric acid, In (JT Baker) (0.031 mL, 1.030 mmol). The reaction was stirred at rt in closed system for 20 min. The reaction mixture was partitioned between EtOAc/sat. NaHCO3. The aqueous layer was extracted with EtOAc (2×10 mL). The combined organic layer were dried over MgSO4 and concentrated. The crude product was purified by column chromatography (24 g, 3% MeOH in DCM) to afford the desired product as a white foam-like solid (135.0 mg). MS (ESI pos. ion) m/z: 244.1. 1H NMR (300 MHz, CDCl3) δ ppm 1.54 (s, 9H) 3.73 (br. s., 2H) 6.93 (br. s., 1H) 7.52 (d, J=2.63 Hz, 1H) 7.94 (d, J=2.63 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-8bd3a173dbf941afa14831e974a6f03c
Source noteuspto-grants-2014_07