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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715898Generated: October 26, 2026

Sodium Bicarbonate → HCID 59465931, compound

https://huagongshe.com/reaction/1715898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant1,2,4-Thiadiazol-5-amine--hydrogen chloride (1/1)HCID 22014543—
Reactant(r)-4-(3-Methylpiperazin-1-yl)-n-(1,2,4-thiadiazol-5-yl)benzenesulfonamideHCID 59465674—
Reactant7-Chloro-indole-1-acetic acidHCID 67082699—
ProductHCID 59465931HCID 59465931288.7%

Reaction Steps

Synthesized according to general procedure 9, method B. The reaction was set up with (R)-4-(3-methylpiperazin-1-yl)-N-(1,2,4-thiadiazol-5-yl)benzenesulfonamide (400 mg, 1.2 mmol), 2-(7-chloro-1H-indol-1-yl)acetic acid (250 mg, 0.15 mmol), HATU reagent (390 mg, 0.15 mmol), sodium bicarbonate (151 mg, 1.8 mmol), and DMF/CH2Cl2-1/1 (1.0 mL) to obtain the desired amide as a white solid (230 mg, 36% yield). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=531.0; tR=3.21 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799822B2
Source datasetuspto-grants-2010_09
ORD IDord-2865b162b89845cc84fbebf3782ef689
Source noteuspto-grants-2010_09