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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096911Generated: November 1, 2026

Hydrochloric Acid → HCID 178433902, compound

https://huagongshe.com/reaction/1096911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-methyl-1-(pyridin-2-yl)-1H-thieno[2,3-c]pyrazole-5-carboxylic acidHCID 43328339—
ReactantHCID 178479612HCID 178479612—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178433902HCID 178433902—

Reaction Conditions

Temperature80 °C

Reaction Steps

6-(Tetrazol-5-yl)spiro[chroman-2,4′-piperidin]-4-one hydrochloride (232 mg), 3-methyl-1-pyridin-2-yl-1H-thieno[2,3-c]pyrazole-5-carboxylic acid (155 mg), EDCI (153 mg) and HOBT (122 mg) were suspended in Et3N (1 mL) and DMF (8 mL). The suspension was stirred at 80° C. for 1.5 hours under heat, then cooled to room temperature, and chloroform (1.8 mL) was added thereto. Its pH was adjusted at 2.5 with 1 N HCl added thereto, and this was diluted with water, and Et2O was added thereto. The formed crystal was taken out through filtration, washed with water and Et2O—CHCl3, and dried in vacuum to obtain the title compound as a pale yellow powder. 1H-NMR (400 MHz, DMSO-d6): δ 8.53 (1H, d, J=4.4 Hz), 8.44 (1H, s), 8.25 (1H, d, J=8.5 Hz), 8.01 (1H, t, J=7.8 Hz), 7.90 (1H, d, J=8.5 Hz), 7.61 (1H, s), 7.37 (1H, d, J=8.8 Hz), 7.31 (1H, t, J=5.9 Hz), 6.44 (2H, s), 4.20 (2H, d, J=12.9 Hz), 3.48 (2H, br s), 2.52 (3H, s), 2.06 (2H, d, J=13.7 Hz), 1.94-1.81 (2H, m). MS [M+H]+=527.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138197B2
Source datasetuspto-grants-2012_03
ORD IDord-d2c4222632cb4b33bf244bf716a0b18a
Source noteuspto-grants-2012_03