Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235076Generated: October 30, 2026

Benzyl Bromide → HCID 23353357, compound

https://huagongshe.com/reaction/235076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 23353262HCID 23353262—
ProductHCID 23353357HCID 2335335762%

Reaction Steps

Ethyl 3-aminothieno[2,3-b]pyrazine-2-carboxylate (0.450 g, 2.02 mmol) was treated with neat NaH (0.058 g, 2.42 mmol) and benzyl bromide (0.380 g, 2.22 mmol) as described in Example 94A. Purification by column chromatography on silica gel eluting with a solvent gradient from 10:1 to 3:1 hexanes:ethyl acetate gave the title compound (0.39 g, 62%) as a yellow solid. 1H NMR (300 MHz, CDCl3) δ1.39 (t, 3H), 4.37 (q, 2H), 5.38 (d, 2H), 7.19-7.42 (m, 5H), 7.88 (br t, 1H), 8.55 (m, 2H). MS (DCI/NH3) m/e 3 14 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597823
Source datasetuspto-grants-1997_01
ORD IDord-06e04dace9cc45f9aacbdc0df4809463
Source noteuspto-grants-1997_01