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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988893Generated: November 2, 2026

1-Hydroxybenzotriazole → 2-(6-bromo-1,2-benzisoxazol-3-yl)-N-(2-hydroxyethyl)acetamide

https://huagongshe.com/reaction/1988893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
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-(6-Bromo-1,2-benzoxazol-3-yl)acetic acidHCID 59127376—
SolventTetrahydrofuranHCID 8028—
Product2-(6-bromo-1,2-benzisoxazol-3-yl)-N-(2-hydroxyethyl)acetamideHCID 58656496—

Reaction Steps

A suspension of (6-bromo-1,2-benzisoxazol-3-yl)acetic acid (Intermediate 32) (0.10 g) and HATU (0.18 g) in tetrahydrofuran (5 ml) was stirred at room temp. for 10 min then treated with 1-hydroxybenzotriazole (0.05 g) 2-aminoethanol (0.03 ml) and diisopropylethylamine (0.2 ml). The mixture was stirred for a further 18 h then concentrated under vacuum. The residue was partitioned between dichloromethane (5 ml) and 2M aqueous sodium carbonate (5 ml). The organic layer was dried using a hydrophobic filter tube then applied to a Varian Bond-Elut SPE cartridge. Sequential elution with dichloromethane, ether, ethyl acetate, acetonitrile and acetone yieldded the title compound as a white solid (0.08 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642276B2
Source datasetuspto-grants-2010_01
ORD IDord-2a15222a0f3b407682fb33e2513c9c2a
Source noteuspto-grants-2010_01