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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507140Generated: October 31, 2026

Bromoacetonitrile → HCID 90376271, compound

https://huagongshe.com/reaction/1507140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 90375023HCID 90375023—
ProductHCID 90376271HCID 90376271—

Reaction Steps

General Procedure T from tert-butyl N-{[4-(aminomethyl)pyridin-2-yl]methyl}-N-[(dimethylcarbamoyl)methyl]carbamate (1.0 equiv.), DIPEA (2.0 equiv.) and bromoacetonitrile (1.1 equiv.). Purification by preparative TLC (10% MeOH and 1% NH4OH in DCM) gave the title product as light yellow oil. 1H NMR (300 MHz, methanol-d4): δ ppm 8.42 (d, 1H), 7.46 (s, 1H), 7.33 (s, 1H), 4.58 (m, 2H), 4.19 (m, 2H), 3.93 (s, 2H), 3.65 (s, 2H), 2.98 (m, 6H), 1.42 (m, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221801B2
Source datasetuspto-grants-2015_12
ORD IDord-d0141e928a834960a5690aabbc1cd051
Source noteuspto-grants-2015_12