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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883709Generated: October 30, 2026

Diisopropylethylamine → HCID 23508314, compound

https://huagongshe.com/reaction/1883709

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—
Reactant2-(2-(O-tolylamino)benzo[d]oxazol-6-yl)acetic acidHCID 23508315—
ReactantHCID 23508318HCID 23508318—
SolventDimethylformamideHCID 6228—
ProductHCID 23508314HCID 23508314104.6%

Reaction Steps

A mixture of 2-(2-o-tolylamino-benzoxazol-6-yl)acetic acid (0.398 g, Reference Example 2), O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (0.59 g) and diisopropylethylamine (0.24 g) in dimethylformamide was stirred at room temperature for 10 minutes and then treated with a solution of ethyl 3-[7-amino-indan-4-yl]-butanoate hydrochloride (0.4 g, Reference Example 5) in dimethylformamide. After shaking and then allowing to stand at room temperature for 16 hours the reaction mixture was evaporated under high vacuum. The residual red oil was dissolved in ethyl acetate and the solution was washed with 5% aqueous sodium bicarbonate, then with water, then dried over sodium sulfate and then evaporated to give the title compound (0.754 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762199B2
Source datasetuspto-grants-2004_07
ORD IDord-37c3801a16e24ff08da15562fe7869e1
Source noteuspto-grants-2004_07