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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883141Generated: October 26, 2026

N-benzyl-2-(4-bromobutanamido)-4-methylthiazole-5-carboxamide → HCID 16954475, compound

https://huagongshe.com/reaction/883141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzyl-2-(4-bromobutanamido)-4-methylthiazole-5-carboxamideHCID 86638730—
Reactant2-(4-bromobutanamido)-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamideHCID 86638731—
ProductHCID 16954475HCID 1695447585%

Reaction Steps

Following the procedure as described in Example 1, making variations as required to use 2-(4-bromobutanamido)-N-(4-fluorobenzyl)-4-methylthiazole-5-carboxamide in replace of N-benzyl-2-(4-bromobutanamido)-4-methylthiazole-5-carboxamide, the title compound was obtained as a white solid in 85% yield: 1H NMR (300 MHz, CD3OD) δ 7.39-7.33 (m, 2H), 7.09-7.02 (m, 2H), 4.48 (s, 2H), 4.15-4.09 (m, 2H), 2.68 (t, J=8.1 Hz, 2H), 2.55 (s, 3H), 2.25 (m, 2H); MS (ES+) m/z 334.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236835B2
Source datasetuspto-grants-2012_08
ORD IDord-2d4fb5d33101441fb45e966a89e18f3a
Source noteuspto-grants-2012_08