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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420667Generated: November 1, 2026

Hydrochloric Acid → HCID 178433880, compound

https://huagongshe.com/reaction/2420667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfamic AcidHCID 5987—
Reactant3-(3-Amino-2-hydroxyphenyl)benzoic acidHCID 11492332—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178429255HCID 178429255—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 178433880HCID 17843388095.4%

Reaction Steps

3′-Amino-2′-hydroxybiphenyl-3-carboxylic acid (“BPCA”) Form I (90 g, 392.6 mmol), was added slowly with stirring at room temperature to a solvent mixture of tech. methanol (1.8 L) and 4 M hydrochloric acid (0.245 L, 981.5 mmol) in 3 L reactor. The resulting red solution was stirred for thirty minutes. The solution was then cooled to 0-5° C. and a cold solution of sodium nitrite (27 g, 391.3 mmol) in 90 mL of water was added over twenty minutes such that the reaction mixture temperature did not rise above 10° C. The reaction mixture was stirred for one hour at 5-10° C. Sulfamic acid (4 g, 41.2 mmol) in 90 mL of water was added at 5° C. and the resulting mixture was stirred for additionally one hour at the same temperature. The reaction mixture was warmed to room temperature and triethylamine (ca 104 mL) was added to adjust pH 7-8. 1-(3,4-dimethylphenyl)-3-methyl-1H-pyrazol-5-ol (“pyrazole”) form I (72 g, 357.8 mmol), was added in one portion to the reaction mixture and the resulting mixture was stirred for additionally two hours at room temperature. Hydrochloric acid (4M, ca 140 mL) was slowly added with stirring over twenty minutes to adjust pH to 1.8. A solid precipitated and was collected by filtration, washed with of mixture MeOH:water (1:1, 100 mL) and dried at 40° C./0 bar in vacuum oven for about 18 hours giving 151 g of crude orange to brown crystals of Eltrombopag crude (XRPD: form III with small percentage (less than 10%) of form I. (HPLC: 98.5%, Yield=95.4%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956048B2
Source datasetuspto-grants-2011_06
ORD IDord-e4b91c21c5274719a6e03c691ce48664
Source noteuspto-grants-2011_06