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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042096Generated: November 2, 2026

2,2,2-Trichloroethyl chloroformate → HCID 67252263, compound

https://huagongshe.com/reaction/2042096

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58851701HCID 58851701—
SolventEthyl AcetateHCID 8857—
ProductHCID 67252263HCID 67252263103.6%

Reaction Steps

To a stirring solution of t-butyl 6-(5-amino-3-t-butyl-1H-pyrazol-1-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate (see WO 2006/071940A2, 0.075 g, 0.20 mmol) and Troc-Cl (0.028 ml, 0.21 mmol) in EtOAc (2 ml) was added sat'd. NaHCO3 (0.82 ml, 0.61 mmol). The resulting biphasic solution was stirred at RT overnight. The layers were separated and the aqueous phase was extracted with EtOAc (2×). The combined organic phases were washed with brine (1×), dried (MgSO4) and concentrated in vacuo to give crude t-butyl 6-(3-t-butyl-5-((2,2,2-trichloroethoxy)carbonyl)-1H-pyrazol-1-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate (0.110 g, 100% yield). 1H NMR (DMSO-d6) δ 9.93 (brs, 1H), 7.29-7.24 (m, 2H), 6.83-6.80 (m, 1H), 6.27 (s, 1H), 4.85 (s, 2H), 4.52 (brs, 2H), 3.57-3.53 (m, 2H), 2.82-2.79 (m, 2H), 1.44 (s, 9H), 1.27 (s, 9H); MS (ESI) m/z: 545.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586565B2
Source datasetuspto-grants-2013_11
ORD IDord-74d7c080b854415a99b89f5857992744
Source noteuspto-grants-2013_11