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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375113Generated: October 28, 2026

Bromoacetic Acid → HCID 135774142, compound

https://huagongshe.com/reaction/2375113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetic AcidHCID 6227—
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 135774127HCID 135774127—
SolventDimethylformamideHCID 6228—
ProductHCID 135774142HCID 13577414235%

Reaction Steps

In a manner analogous to that of Example 19, to a stirred suspension of 8-amino-1,5-dihydro-6H-[1,2]diazepino[4,5,6-cd] indol-6-one hydrochloride in anhydrous N,N-dimethylformamide (9 mL) was added bromoacetic acid (168 mg. 1.2 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (553 mg, 1.4 mmol) and triethylamine. The reaction was stirred at room temperature for 16 hours. The volatile components were evaporated and water was added to the residue. The precipitated orange solids were collected by filtration and washed with water and ethyl acetate. After drying, the title compound (158 mg) was obtained as an orange powder in 35% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462713B2
Source datasetuspto-grants-2008_12
ORD IDord-acf0b9470f6a41c9a2022bf01af79474
Source noteuspto-grants-2008_12