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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678248Generated: November 1, 2026

Triethylamine → (7-benzo[b]thiophen-2-yl-1H-indazol-5-yl)-thiocarbamic acid S-methyl ester

https://huagongshe.com/reaction/1678248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl chloromethanethioateHCID 554404—
ReactantHCID 59023728HCID 59023728—
SolventEthanolHCID 702—
Product(7-benzo[b]thiophen-2-yl-1H-indazol-5-yl)-thiocarbamic acid S-methyl esterHCID 5902385466%

Reaction Steps

To a solution of 7-benzo[b]thiophen-2-yl-1H-indazol-5-ylamine (Example #F.8.1, 530 mg, 2.0 mmol) and methyl chlorothioformate (0.25 mL, 2.8 mmol) in ethanol (10 mL) was added triethylamine (0.56 mL, 4.0 mmol). The reaction mixture was stirred at ambient temperature for about 16 hours and the resulting solid was collected by filtration, washed with water (3×50 mL), and dried to yield (7-benzo[b]thiophen-2-yl-1H-indazol-5-yl)-thiocarbamic acid S-methyl ester (448 mg, 66%); LC/MS (Table 1, Method e) Rt 2.14 min; m/z: [M−H]− 338.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008481B2
Source datasetuspto-grants-2011_08
ORD IDord-e270663c97304f4bb9384348b20cbc6c
Source noteuspto-grants-2011_08