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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199704Generated: October 29, 2026

1,2-Dichloroethane → HCID 46853084, compound

https://huagongshe.com/reaction/2199704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant(1H-tetrazol-5-ylmethyl)amineHCID 5146781—
ReactantHCID 58513017HCID 58513017—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 46853084HCID 46853084—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 4-{(1S)-1-[(7-bromo-5-methyl-1-benzothien-3-yl)(4-chlorophenyl)methyl]butyl}benzoic acid (EXAMPLE 3, Step A, 20.0 mg, 0.038 mmol), 1-(2H-tetrazol-5-yl)methanamine (10.9 mg, 0.110 mmol), EDC (22.0 mg, 0.110 mmol), HOBt (17.0 mg, 0.110 mmol) and DIEA (0.050 mL, 0.29 mmol) in DMF (1 mL) was heated at 65° C. for 12 hours. The mixture was allowed to cool to RT, diluted with acetonitrile, then purified by preparative reverse-phase HPLC eluting with 38-100% acetonitrile/water+0.1% TFA. Following lyophilization, this afforded the title compound as a white solid. 1H NMR (500 MHz, d6-DMSO) δ 9.04 (br, 1H); 7.96 (s, 1H); 7.84 (s, 1H); 7.67 (d, J=8 Hz, 2H); 7.64 (d, J=8 Hz, 2H); 7.52 (d, J=8 Hz, 2H); 7.39 (d, J=8.5 Hz, 2H); 7.35 (br, 1H); 4.84 (d, J=11.5 Hz, 1H); 4.67 (d, J=5.5 Hz, 2H); 3.74 (t, J=12 Hz, 1H); 2.40 (s, 3H); 1.44-1.52 (m, 1H); 1.24-1.32 (m, 1H); 0.91 (q, J=7.5 Hz, 2H); 0.67 (t, J=7 Hz, 3H). LC2: 2.63 min. (M+H)+ 608.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359339B2
Source datasetuspto-grants-2016_06
ORD IDord-fe9cf3ca8eb340a48910218d5b7093aa
Source noteuspto-grants-2016_06