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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169138Generated: November 2, 2026

HCID 178484642, compound → HCID 178484641, compound

https://huagongshe.com/reaction/2169138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178484642HCID 178484642—
ReactantHCID 178484772HCID 178484772—
ProductHCID 178484641HCID 17848464161.4%

Reaction Steps

5-Benzyloxy-2-(2′-chloro-biphenyl-2-ylmethyl)-6-hydroxypyrimidine-4-carboxylic acid (2-hydroxyethyl)-methyl-amide (10-02) (1 g, 61.34%) was synthesized as a yellow liquid from 5-benzyloxy-2-(2′-chloro-biphenyl-2-ylmethyl)-6-hydroxypyrimidine-4-carboxylic acid [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-methyl-amide (9-02) (2 g, 3.23 mmol) following the procedure as described for 5-benzyloxy-2-biphenyl-2-ylmethyl-6-hydroxypyrimidine-4-carboxylic acid (2-hydroxyethyl)-methyl-amide (10-01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-74ca1d8fed224a99b907e639a80c7994
Source noteuspto-grants-2015_06