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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916253Generated: October 31, 2026

2-Chloro-5-methylpyrimidine → HCID 55299071, compound

https://huagongshe.com/reaction/1916253

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-methylpyrimidineHCID 581719—
Reactant2-Chloro-4-methylpyrimidineHCID 11629607—
ProductHCID 55299071HCID 55299071—

Reaction Steps

Compound P17 was prepared according to the general procedure for the synthesis of P12 described in Preparation 51, except that 2-chloro-4-methylpyrimidine (the synthesis of 2-chloro-4-methylpyrimidine is described by D. B. Harden & M. J. Mokrosz, J. Organic Chem., 1998, 53, 4137-4140) was used instead of 2-chloro-5-methylpyrimidine, to provide P17. Yield: 647 mg, 4.34 mmol, 87%. 1H NMR (400 MHz, CD3OD) δ 2.52 (s, 3H), 4.0 (m, 2H), 4.12 (m, 2H), 4.18 (m, 1H), 7.23 (d, J=5.4 Hz, 1H), 8.59 (d, J=5.4 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618117B2
Source datasetuspto-grants-2013_12
ORD IDord-54c638a19604410e9a344f7a6a3f9b1c
Source noteuspto-grants-2013_12