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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169341Generated: October 31, 2026

Diisopropylethylamine → HCID 178455248, compound

https://huagongshe.com/reaction/2169341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant[2-(tert-Butyl-dimethylsilanyloxy)-ethyl]-cyclopropylmethyl-amineHCID 69361897—
ReactantHCID 178524866HCID 178524866—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 178455248HCID 178455248120.1%

Reaction Steps

To a stirred solution mixture of 5-benzyloxy-6-hydroxy-2-(1-phenyl-cyclopentylmethyl)-pyrimidine-4-carboxylic acid (283) (250 mg, 0.62 mmol) and [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-cyclopropylmethyl-amine (8i) (170 mg, 0.74 mmol) in dimethylformamide (3 mL) were added N,N-diisopropylethylamine (0.3 mL, 1.85 mmol) and HATU (352 mg, 0.93 mmol). The reaction mixture was stirred at room temperature for 20 h. Water (75 mL) was added and the mixture was extracted with ethyl acetate (3×20 mL). The combined organic part was washed with water (3×50 mL) and brine (2×30 mL) and dried and concentrated. The crude product was purified by Combi-Flash column (eluted at 20-30% ethyl acetate in hexane) to get 5-benzyloxy-6-hydroxy-2-(1-phenyl-cyclopentylmethyl)-pyrimidine-4-carboxylic acid 5-benzyloxy-6-hydroxy-2-(1-phenyl-cyclopentylmethyl)-pyrimidine-4-carboxylic acid [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-cyclopropylmethyl-amide (304) (380 mg, 99.82%) as a light yellow sticky solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-8e6774761eef461ca42baee03f28b614
Source noteuspto-grants-2015_06